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Review

Trichoscopy and Computational Models for Hair and Scalp Disorders: Image Analysis, Quantification, and Clinical Integration

by
Corrado Zengarini
1,2,†,
Nico Curti
3,*,†,
Stephano Cedirian
1,2,
Luca Rapparini
1,2,*,
Francesca Pampaloni
1,2,
Alessandro Pileri
1,2,
Francesco Durazzi
3,
Martina Mussi
1,2,
Michelangelo La Placa
1,2,‡,
Bianca Maria Piraccini
4,‡ and
Michela Starace
1,2,‡
1
Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy
2
Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy
3
Department of Physics and Astronomy, University of Bologna, 40127 Bologna, Italy
4
Private Dermatology Practice, 40137 Bologna, Italy
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
These authors contributed equally to this work.
Appl. Sci. 2026, 16(7), 3199; https://doi.org/10.3390/app16073199
Submission received: 1 February 2026 / Revised: 14 March 2026 / Accepted: 24 March 2026 / Published: 26 March 2026

Featured Application

This review is intended as a roadmap for clinicians and researchers interested in trichoscopy-centered computational imaging for hair and scalp disorders. It compares available digital systems and algorithmic strategies, summarizing performance metrics and discussing practical implementation in clinical workflows.

Abstract

This scoping review summarizes current computational image analysis and artificial intelligence (AI) approaches for the assessment of hair and scalp disorders, with emphasis on quantitative trichoscopy and operator-independent evaluation. A deep Medline search was performed using a citation network-based approach using MeSH terms and complementary keywords covering diagnostic imaging, trichoscopy/videodermoscopy, image processing, algorithms, AI, and mobile/smartphone-based workflows. Overall, relatively few studies assess algorithms in real-world clinical pathways, and much of the retrieved literature is predominantly pre-clinical or methodology-driven. In parallel, commercially available AI-assisted trichoscopy platforms have little or no traceable peer-reviewed evidence; their validation methods and underlying datasets are often proprietary, undisclosed, and not directly comparable, limiting independent verification and cross-platform benchmarking. The most mature academic applications focus on follicular unit quantification (hair density, shaft diameter distribution, vellus-to-terminal ratio, and severity mapping), mainly using convolutional neural networks with object detection and instance segmentation. In conclusion, AI-assisted trichoscopy may support a shift toward standardized quantitative outputs, but clinical translation remains early and constrained by small or proprietary datasets, heterogeneous acquisition/annotation protocols, limited external validation, and scarce prospective studies.

1. Introduction

The hair follicle (HF) is a highly specialized, self-renewing mini-organ that cycles through defined stages of anagen, catagen, telogen, latency, and miniaturization, making it an ideal model system for studying tissue dynamics and systems biology [1]. Each follicle operates as an independent biological entity capable of undergoing complete regenerative cycles, yet in human scalp skin, follicles are not randomly distributed, but rather organized into follicular units (FUs), i.e., compact anatomical and functional clusters comprising one to four terminal hair follicles that share a common pilosebaceous apparatus, vascular network, and arrector pili muscle insertion.
Each FU typically comprises one to four terminal hairs (depending on genetic predisposition and scalp location), associated sebaceous glands, an arrector pili muscle, and a shared infundibular ostium. This architectural and functional complexity enables remarkable regenerative capacity but also renders the HF susceptible to multiple regulatory failures that underlie the most common hair disorders [2,3].
Dysregulation of the hair cycle can result in a wide range of clinical presentations, among the most common androgenetic alopecia (AGA), characterized by progressive follicular miniaturization and a shortened anagen phase [4,5] and alopecia areata (AA), an autoimmune condition causing non-scarring hair loss [6,7,8]. Accurate assessment of these changes is critical, as subtle variations in hair shaft diameter, follicular density, and anagen–telogen ratio often precede visible clinical signs [9].
Therefore, not only qualitative but quantitative evaluation of the FU and its dynamics is essential for diagnostic classification but also for monitoring disease progression and therapeutic response over time [10,11,12].
In clinical and research settings, follow-up of the main follicular and hair parameters, such as hair shaft diameter, hair count per cm2, proportion of vellus versus terminal hairs, and hair growth rate, is the cornerstone for monitoring and evaluating treatment efficacy in alopecic conditions [13,14]. To address this, a variety of systems have been developed over the years to perform quantitative analysis, ranging from early analogue and digital phototrichograms to modern high-resolution trichoscopic devices [15,16]. Traditional methods include manual hair counting on magnified scalp images, ink-marking of defined scalp areas (unit-area trichogram), and cross-sectional trichometry for measuring mean hair thickness [17,18]; it is imaginable that these methods are intra- and inter-operator variable, time-consuming, and often less reliable. Later, semi-automated solutions combined digital imaging with algorithmic hair segmentation, but initially these advances still relied on supervised correction and validation by expert operators, often involving labor-intensive frame-by-frame hair counting or manual delineation of analysis areas [19]. This operator dependence not only introduced subjectivity but also limited reproducibility, particularly in teledermatology and multicenter trials, where standardization is crucial [20].
Finally, artificial intelligence (AI) and deep learning (DL) have been heavily implemented as transformative tools to overcome these constraints by automating follicle detection, segmentation, and classification to derive density and growth metrics. This has already been implemented in semi-supervised and unsupervised digital tools such as standalone tools or plugins in digital dermato/trichoscopic devices [19]. Such systems drastically reduce observer variability while providing highly reproducible quantitative data, and are based mainly on convolutional neural networks (CNNs), object detection frameworks such as YOLOv4, EfficientNet, and DetectoRS, as well as instance segmentation architectures like Mask R-CNN, and have been trained on large trichoscopic datasets to compute follicular density, shaft diameter distribution, and local severity mapping. These approaches potentially enable more automated and operator-independent analysis and longitudinal follow-up. The reachable potential is to have highly reproducible quantitative data and to reduce observer variability compared with manual evaluation.
Collectively, these innovations mark a paradigm shift from descriptive trichoscopy to quantitative, standardized, and reproducible digital trichology.
Building upon this evolution, the present scoping review aims to provide clinicians and researchers with a structured overview of the current AI-based analytical systems applied to hair and scalp disorders, focusing on the current research trends/topics and highlighting the current missing directions that could be addressed by future research.

2. Materials and Methods

A scoping literature search was conducted on the PubMed database to identify publications on hair diseases assessed using diagnostic imaging and advanced digital methods. The Boolean operators AND/OR were used to combine the terms and maximize sensitivity. To automatically evaluate the current research trends, we proposed a novel search approach, building a citation network from the most common and informative MeSH terms in literature. We downloaded the full PubMed database from the official repository, containing scientific papers published up to 2 October 2025. We used the reported MeSH identifiers to extract the papers’ topics and match those of interest, with the MeSH identifier being the list of topics assigned to each paper by PubMed. We considered as relevant papers those assigned MeSH identifiers matching the following query: (hair diseases/diagnostic imaging OR hair/diagnostic imaging OR hair follicle OR dermatoscopes) AND (machine learning OR artificial intelligence OR software OR algorithm OR image-processing, computer-assisted, mobile-applications, smartphone). We restricted our analysis to the PubMed database only since it provides robust and well-structured APIs for our automated search.
The search was restricted to English-language studies, and all identified records were assessed for eligibility according to PRISMA guidelines. No exclusion criteria were implemented for conference papers or proceedings. Literature results were extracted using a network-based approach combined with custom machine-learning software for the identification of related topics/keywords. The set of articles and associated data was independently reviewed by two independent experts to ensure accuracy and reduce bias. Any disagreements were resolved by discussion or consultation with a third reviewer.

Citation Network Analysis

Using the papers extracted with this procedure, we built a citation network, connecting the selected papers according to their citations, i.e., we considered a network link from a paper to another when the first cited the latter [21,22]. Each node of the obtained network, i.e., a paper, was analyzed using a Natural Language Processing (NLP) pipeline: selecting the title and abstract sentences, we pre-processed the text, discarding the irrelevant words (rejection criteria, e.g., conjunctions, adjectives, adverbs, etc.), identifying a subset of 5 keywords which identified as best as possible the topic discussed in the work [23,24].
Starting from this network structure, a graph-based analysis was performed, evaluating the presence of possible disjoined connected components and centrality measurements: the “literature importance” of a paper could be quantified by the number of papers which cited it (i.e., a degree centrality of the node graph), or by its importance in connecting two highly dense components (i.e., the betweenness centrality of the node graph). This approach helps us in identifying the most relevant and central research, with the possibility of discarding novel articles or works which propose simply improving available techniques. We would like to stress that in our review, we are mainly interested in covering the principal and/or missing topics about these arguments, and a paper which produces a unique citation does not represent a significant improvement in our discussion.
Furthermore, a community detection analysis was performed according to the Louvain method, aiming to identify collections of topics and possible gaps in literature organization, i.e., the absence of direct connections between communities of different arguments which highlight missing documentations of longitudinal topics. Default resolution parameters were used, and the resulting communities were interpreted as thematic clusters representing groups of papers sharing similar citation patterns [25]. Potential sources of bias were considered during study appraisal; however, a formal tool-based risk-of-bias table is not reported due to limited applicability across the heterogeneous study designs included. The entire list of papers identified by our method, alongside the data about their positioning in the network structure, was manually analyzed by two independent reviewers to guarantee the correctness of the extracted information.

3. Results

The search strategy yielded 1261 records through the Medline database. Due to the single database search, no duplicates could be included. We conducted a preliminary screening of titles and abstracts, and potentially relevant articles were assessed for eligibility according to predefined inclusion and exclusion criteria automatically checked by our search system. We remark that the principal exclusion criteria implemented involved the removal of articles linked to the others (core) with a single and unique citation.
Following full-text evaluation, 58 studies met the inclusion criteria and were retained for qualitative synthesis. The main reasons for exclusion included:
Studies focusing exclusively on basic biological or molecular mechanisms without imaging or AI method implementation;
Animal or in vitro investigations not translatable into clinical or imaging settings;
Reports addressing hair growth or follicle physiology without the use of diagnostic imaging or computational analysis;
Studies lacking quantitative or visual diagnostic data relevant to trichoscopic or dermoscopic evaluation.
The PRISMA flow diagram [Figure 1] summarizes the selection process:
  • Records identified through database searching: 1261;
  • Records after screening and eligibility assessment: 58 included;
  • Records excluded: 1203.
This process ensured the inclusion of the most relevant publications addressing imaging and computational and AI applications in the evaluation of hair and scalp disorders.
  • Results—Citation network
The pruned citation network consisted of 58 nodes (articles) and 91 edges, where each edge represented a shared citation between pairs of studies. This pruning process reduced a larger initial selection/network to its most informative structure (core), retaining articles with meaningful bibliographic similarity while improving interpretability and reducing noise [Figure 1] [26].
Overall, the network showed moderate connectivity, with a mean node degree of 3.1, indicating that each article shared approximately three common references with other studies on average. The degree distribution was right-skewed, with a small number of highly connected nodes (maximum degree = 17) acting as hubs, and a larger number of peripheral articles with few shared citations. This pattern suggests the presence of influential or methodologically central publications that bridge multiple thematic areas.
Betweenness centrality values were generally low (mean ≈ 0.04), indicating that most articles contributed locally to knowledge clusters rather than serving as dominant global bridges. However, a limited subset of nodes exhibited higher betweenness, highlighting their role in connecting otherwise distinct research themes.
Community detection identified seven distinct communities, reflecting coherent thematic groupings of articles based on shared citation patterns. Community sizes ranged from 4 to 12 articles, indicating both well-established and more specialized research strands within the field.
The communities were meaningfully associated with the MeSH descriptor profiles of the articles:
  • Larger communities were characterized by methodological and technological descriptors, such as Algorithms, Neural Networks, Computer-Assisted Image Analysis, and Radiography, reflecting clusters of studies focused on automated or imaging-based hair assessment.
  • Other communities showed stronger associations with clinical and biological descriptors, including Hair Follicle, Scalp, Alopecia, Humans, and sex-specific terms, suggesting clinically oriented research groups.
  • Smaller communities appeared more specialized, often combining niche methodological approaches with specific clinical applications.
  • The separation between communities, combined with limited cross-community connectivity, indicates that while the field shares common methodological foundations, research remains partially compartmentalized into subdomains with distinct citation traditions.
At the node level, highly connected articles tended to combine broad methodological descriptors with clinical relevance, positioning them as reference points across multiple communities. In contrast, low-degree nodes often corresponded to more recent or narrowly focused studies, contributing depth within specific subtopics rather than breadth across the network [Figure 2].
  • Data synthesis
The final dataset of 58 studies [Appendix A], published between the earliest identified record and September 2025, reflects the progressive integration of digital technologies in trichology.
The included literature encompasses both quantitative and qualitative investigations focusing on diagnostic imaging, computer-assisted analysis, and AI-based tools for hair disease assessment.
To show the actual state of the art, results synthesis was organized into three main conceptual domains:
  • Studies on the pre-clinical features of scalp diseases:
    Biological and histological models assessing and targeting scalp diseases causes and pursuing diagnostical models.
  • Computer-assisted and algorithmic methods:
    Research employing image processing and software-driven analysis for segmentation, measurement, and morphological characterization of follicular structures.
    Studies developing or validating AI algorithms for pattern recognition, disease classification, and automated image interpretation in trichoscopy.
  • Software implementing AI techniques:
    Works exploring portable trichoscopy, smartphone-based imaging, and remote diagnostic workflows integrating artificial intelligence or cloud-based analytics.
Studies on the pre-clinical feature of scalp diseases using imaging and computational models.
  • Omics aspects of the HF
The HF provides a unique model for exploring tissue-level dynamics and molecular regulation of hair cycling. Computational approaches, such as follicular automaton, simulate stochastic transitions of thousands of follicles across the anagen, catagen, and telogen stages, effectively reproducing the graded patterns observed in androgenetic alopecia [27].
At the molecular level, studies have elucidated the central role of Wnt/β-catenin signaling in controlling the telogen-to-anagen transition [28,29]. Telomerase reverse transcriptase (TERT) also promotes anagen independently of its catalytic activity, inducing proliferation within the interfollicular epidermis and engaging transcriptional programs overlapping with Myc and Wnt signaling [30].
Chronobiological regulation also plays a critical role in follicular function: hair follicles possess peripheral circadian clocks, and gene expression can be measured noninvasively from plucked hair samples, allowing accurate monitoring of circadian phase [31,32].
2.
Structural model of the HF
High-resolution imaging techniques provide unprecedented structural and molecular insight into hair follicles: three-dimensional reconstruction of serially sectioned tissue, complemented by Micro CT, has refined our understanding of the arrector pili (AP) muscle. The AP is now recognized as a single, branched muscular structure that aligns with follicular orientation and inserts into all follicles within a follicular unit, with quantifiable metrics for depth and length in intact skin [33,34].
3.
Main limitations
Organ-cultured human hair follicles have been pivotal for mechanistic studies [35]. Nevertheless, a major limitation remains: the reliance on murine models, which fail to replicate key human-specific pathologies. These challenges underscore the importance of human-centered models, such as organ-cultured follicles and bioengineered skin systems, despite technical limitations in monitoring follicular miniaturization and regeneration [36].
  • Computer-assisted algorithmic methods
AI applications, particularly deep learning, have been pivotal in moving hair pathology diagnosis from qualitative assessment toward precise, quantitative measurement regarding the external aspects of the FU. Modern DL algorithms focus on reliably detecting and classifying hair follicles, overcoming limitations associated with overlapping shafts, image noise, and variable acquisition conditions.
Comparative studies evaluating object detection frameworks, such as YOLOv4, EfficientDet, and DetectoRS, have demonstrated the feasibility of automated HDM. YOLOv4 achieved the highest detection performance, with a mean Average Precision (mAP) of 58.67% and reduced rates of redundant follicle detection [37].
More complex DL models, including Mask R-CNN with ResNet-101 feature extraction, have been employed to segment follicles and classify them into clinically relevant categories—healthy, normal, or severe—based on parameters such as follicle size, hair count, and thickness. These models generate local hair loss severity indices (P) and aggregate severity maps (Pavg) that can be visualized as heatmaps, providing a spatial overview of hair loss progression across the scalp [37] [Figure 3].
Beyond follicle-level quantification, DL-based classifiers have demonstrated high accuracy in multi-disorder categorization. An enhanced Xception-based network achieved a diagnostic accuracy of 92% across six scalp and hair conditions, including alopecia, folliculitis, dissecting cellulitis, effluvium, psoriasis, and acne keloidalis nuchae [38]. Early methods combining Grid Line Selection and eigenvalue computation to extract hair loss features (HLFs) from smartphone-acquired microscopy images also demonstrated an average accuracy of 96.51% for hair count, illustrating the potential for AI-assisted self-monitoring of alopecia [39].
A key advantage of these systems is their objectivity and reproducibility, which reduce inter-clinician variability and improve longitudinal tracking of hair disorders. The adoption of explainable AI (XAI) techniques, such as Grad-CAM and saliency mapping, further enhances interpretability by visualizing which features influence network decisions, a critical requirement for clinical integration [38] [Table 1].
  • Software implementing AI processes
Early proof-of-concept work and available consumer apps demonstrated the feasibility of portable, smartphone-assisted trichoscopy as a technological precursor to current commercial AI-driven platforms.
Most of these systems were primarily designed for local image acquisition and transmission to remote specialists for manual evaluation, without standardized algorithms or public datasets, and the reported outcomes focused on hair density and shaft-diameter estimation, as well as diagnostic concordance between on-site and remote assessments.
Ground-truth validation in these studies relied exclusively on manual expert annotation, with no histologic or cross-device calibration. Despite methodological limitations, these experiments established the conceptual foundation for tele-trichoscopy and digital data capture in trichology [Table 2].
For completeness, this section also includes a qualitative synthesis of commercially available AI-assisted trichoscopy platforms, which, although not systematically represented in PubMed-indexed literature, constitute an integral part of the current diagnostic landscape.
  • Considerations and limits on the software and algorithms reviewed
The analysis of AI-driven trichoscopy software highlights a clear dichotomy between academic, algorithm-focused studies and commercially available platforms. Academic studies predominantly aim to validate specific computer-assisted or deep learning methods under controlled conditions, often focusing on a single diagnostic task such as hair density measurement, follicle detection, or severity classification. These works typically rely on relatively small, single-center datasets, with ground truth defined by expert manual annotation and internal validation procedures.
In contrast, commercial platforms integrate AI algorithms into end-to-end diagnostic ecosystems that combine image acquisition hardware, cloud-based analytics, and automated reporting. While these systems offer clear advantages in terms of usability, real-time feedback, and scalability, their validation strategies frequently rely on proprietary datasets and internal quality assurance processes that are not independently verifiable. As a result, direct methodological comparison with academic models is often not feasible.
Another relevant consideration is that most AI-based software systems, both academic and commercial, focus on external follicular unit features, such as hair density, shaft diameter, vellus-to-terminal ratio, and growth phase estimation. Although these parameters are clinically relevant, they represent indirect surrogates of hair pathology and may not fully capture the biological complexity of follicular disorders. Furthermore, differences in image acquisition protocols, magnification, lighting, and scalp preparation introduce variability that may limit cross-platform reproducibility.
Finally, while explainable AI techniques and user-friendly visual outputs (e.g., heatmaps, severity indices) improve interpretability and clinical acceptance, their implementation remains heterogeneous. Only a minority of systems explicitly report explainability strategies or formally assess their impact on diagnostic confidence and decision-making.

4. Discussion

This review shows that image analysis and artificial intelligence are moving toward progressively reshaping scalp and hair disorder disease assessment, mainly by shifting from qualitative interpretations to more reproducible quantitative outputs. However, the current evidence is still driven by a limited number of datasets, which are often proprietary, restricted-access, or not publicly disseminated. As a result, the few academic non-profit studies and the several software tools and commercial applications developed are based mostly on small and non-transparent databases, making independent verification difficult and slowing meaningful cross-study benchmarking.
Across the retrieved literature, the most mature and reproducible use cases remain follicular unit quantification—hair density, shaft diameter distribution, vellus-to-terminal ratio, and severity mapping—typically implemented through object detection and instance segmentation pipelines. Importantly, these computational approaches are not unique to trichology: the same methodological backbone has already been widely adopted in dermatologic imaging, including melanoma assessment, aesthetic skin analysis, and chronic wound quantification. In this sense, trichoscopy follows an established technological trajectory rather than represents a completely novel AI domain.
Artificial intelligence–driven image analysis has advanced to a more mature stage in several dermatological domains [45], particularly melanoma detection, psoriasis severity assessment, and wound care monitoring [46,47,48,49,50]. In these areas, the availability of large annotated datasets, standardized imaging protocols, and shared benchmarking initiatives has enabled the development and validation of robust deep-learning models. This progress is also partly related to the broader clinical relevance of these conditions. For example, melanoma screening is a cornerstone of dermatological practice, while psoriasis, due to its high prevalence in the general population, attracts strong clinical and research interest across multiple disciplines [51,52]. Moreover, from a diagnostic perspective, these conditions often involve relatively well-defined classification tasks or measurable outcomes, such as distinguishing melanoma from benign lesions or quantifying psoriasis severity scores [53]. For instance, melanoma classification systems trained on dermoscopic repositories have demonstrated high diagnostic performance in controlled settings, while AI approaches in wound care are increasingly applied for automated segmentation, tissue classification, and longitudinal monitoring of chronic wounds [54,55,56].
Nevertheless, the methodological frameworks used in trichoscopic AI—such as convolutional neural networks for object detection, instance segmentation, and image classification—are closely aligned with those already established in other dermatological imaging fields [57]. Therefore, the experience gained in melanoma imaging, psoriasis assessment, and wound care analytics may provide a useful roadmap for future developments in AI-assisted trichoscopy, particularly through the creation of shared datasets, harmonized acquisition protocols, and transparent validation frameworks [58,59,60].
As said, the major limitation is that even when data are available, studies remain difficult to compare. Target definitions, acquisition protocols, annotation procedures, and evaluation metrics are highly heterogeneous, and only a minority of reports clearly describe both the number of images and the number of patients. Ground truth is almost always based on single-center expert annotation, rather than harmonized multi-center reference standards, increasing the risk of center-specific bias and reducing generalizability across devices and populations. For clinical translation, the field would benefit from shared benchmarking datasets (or at least interoperable evaluation frameworks), device-aware calibration, and standardized reporting of dataset composition and annotation quality.
We also acknowledge that the network-based pruning approach possibly discards good-quality papers that are too peripheral or too recent. While this approach is out of the standard for traditional systematic reviews, it may actually enhance the quality of a scoping review, allowing the selection of the core literature for the topic of interest, discarding too-niche or too-recent literature which may become influential in the future but does not reflect the broad scope of the current knowledge.
Beyond measurement tasks, a smaller body of academic work has explored AI systems aimed at multi-condition scalp disease classification and diagnostic decision support. While these studies suggest technical feasibility, they remain far from real-world adoption: labels are inconsistent, external validation is rare, and performance is seldom tested in prospective “human-in-the-loop” settings where clinicians interact with the tool under routine constraints. At present, diagnostic AI in trichology should therefore be interpreted as an emerging academic direction rather than a validated real-life solution, since external validation remains limited, prospective studies assessing workflow integration are scarce, and real-world clinical performance has yet to be robustly established.

5. Conclusions

Artificial intelligence is increasingly supporting scalp image assessment by converting trichoscopic and clinical photographs into quantitative, more reproducible outputs. Most current approaches are measurement-driven and rely on established computer vision architectures (such object detection and instance segmentation for follicular unit quantification [61,62]) like those already widely adopted in other dermatologic imaging fields (e.g., melanoma assessment, aesthetic skin analysis, wound measurement [54,63,64,65]).
AI-assisted trichoscopy represents the most clinically actionable domain, enabling automated extraction of follicular metrics such as hair density, shaft diameter distribution, and vellus-to-terminal ratio, and providing intuitive outputs (e.g., severity heatmaps) that may facilitate follow-up and longitudinal monitoring. However, translation remains constrained by the limited number of available datasets, which are often proprietary or restricted-access and have served as the basis for several software tools and commercial applications. Even when data are reported, heterogeneity in acquisition protocols, annotation rules, and evaluation metrics limit comparability and reduces reproducibility across studies.
In contrast, AI systems aimed at multi-condition scalp disease classification and diagnostic decision support remain largely academic proof-of-concept efforts, with limited external validation and scarce prospective testing in real-world workflows. Future progress will depend on standardized imaging procedures, transparent reporting of dataset composition and annotations, and shared benchmarking frameworks enabling robust cross-device and cross-center validation aligned with clinically meaningful endpoints.

Author Contributions

Conceptualization, C.Z. and M.S.; methodology, N.C., C.Z. and M.S.; software, N.C.; validation, C.Z., N.C., L.R. and F.D.; formal analysis, N.C. and C.Z.; investigation, C.Z., L.R., F.D. and S.C.; resources, M.S., B.M.P., M.L.P. and A.P.; data curation, C.Z., L.R. and F.D.; writing—original draft preparation, C.Z.; writing—review and editing, C.Z., M.S., M.M.; F.P.; N.C., L.R. and F.D. (with input from all authors); visualization, C.Z. and N.C.; supervision, M.S., B.M.P. and M.L.P.; project administration, M.S. and C.Z.; funding acquisition, B.M.P. and M.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the University of Bologna.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are available from the corresponding authors upon reasonable request.

Acknowledgments

The authors would like to thank all colleagues who provided administrative and technical support during data collection and manuscript preparation. During the preparation of this manuscript, the authors used Grammarly (version n 1.154.0.0) to improve the English language and readability. The authors reviewed and edited the output and take full responsibility for the content of this publication. During the study, the authors also used custom machine-learning software to support literature screening and citation-network analyses; all records and extracted data were subsequently checked by human reviewers.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
HFHair Follicle
FUFollicular Unit
AGAAndrogenetic Alopecia
AAAlopecia Areata
AIArtificial Intelligence
DLDeep Learning
CNNConvolutional Neural Network
YOLOv4You Only Look Once v4
EfficientDetEfficientDet (object detection framework)
DetectoRSDetectoRS (object detection framework)
Mask R-CNNMask Region-Based Convolutional Neural Network
XAIExplainable Artificial Intelligence
NLPNatural Language Processing
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
MeSHMedical Subject Headings
mAPmean Average Precision
BASPBasic and Specific (classification system)
IRSIInfrared Spectral Imaging
Micro-CTMicro–Computed Tomography
APArrector Pili (muscle)
TRPV1Transient Receptor Potential Vanilloid 1
TGF-β2Transforming Growth Factor beta 2
TERTTelomerase Reverse Transcriptase
T4Thyroxine

Appendix A

PMIDTitleFirst AuthorJournalYearStudy DesignSettingKey Inclusion Criteria/Case DefinitionIntervention/Exposure/Index TestMain Outcomes
18208333 [30]TERT promotes epithelial proliferation through transcriptional control of a Mycand Wnt-related developmental program Choi JPLoS Genet2008Transgenic mouse + microarrayMouse skin (biopsies)Resting HF stem cells in skinTERT(ci) mutant (RT-independent)TERT activates Myc/Wnt program; stimulates proliferation of keratinocytes/HF anagen
11442744 [66]A comprehensive guide for the accurate classification of murine hair follicles in distinct hair cycle stages Müller-Röver SJ Invest Dermatol2001Histological standardizationMurine dorsal skinBack skin in synchronized cycleHistology + IHC markers (Ki67, etc.)Guida standard per stadiazione ciclo HF (telogen-anagen-catagen)
10504436 [67]A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis Paus RJ Invest Dermatol1999Morphological guideMouse embryosHF development stagesHistology, IHC, enzyme activity10 stages from placode to hair filament; for mutant analysis
15793280 [35]A hot new twist to hair biology: involvement of vanilloid receptor-1 (VR1/TRPV1) signaling in human hair growth controlBodó EAm J Pathol2005Organ culture + IHCHuman scalp HF ex vivoAnagen HFs, ORS keratinocytesCapsaicin stimulationTRPV1 activation inhibits proliferation, and induces catagen via TGF-β2
24005054 [68]A meeting of two chronobiological systems: circadian proteins Period1 and BMAL1 modulate the human hair cycle clock Al-Nuaimi YJ Invest Dermatol2014Ex vivo knockdownHuman HF organ cultureScalp HFs from femalessiRNA vs. BMAL1/Per1Circadian genes BMAL1/Per1 regulates HF growth
16637886 [33]A new model for the morphology of the arrector pili muscleTamatsu YJournal of Anatomy2006Anatomical reconstruction studyLaboratoryScalp skin containing complete follicular units with arrector pili (AP) musclesSerial sectioning and 3D reconstruction of AP muscle morphologyAP muscle forms a single oblique band attaching to multiple follicles within one follicular unit, challenging classic one-muscle–one-follicle model
17596168 [69]A study of the secretion mechanism of the sebaceous gland using three-dimensional reconstruction to examine the morphological relationship between the sebaceous gland and the arrector pili muscleSong WCBritish Journal of Dermatology2007Anatomical/3D reconstruction studyLaboratoryHuman scalp skin containing sebaceous glands and arrector pili muscle3D computer reconstruction to analyze gland–muscle relationshipsSebaceous gland ducts open directly onto hair shaft below arrector pili insertion, supporting holocrine secretion model
26971464 [70]Alopecia areata: Animal models illuminate autoimmune pathogenesis and novel immunotherapeutic strategies Gilhar AAutoimmun Rev2016Review (models)Mouse xenograftsHuman AA grafts to SCID miceJAKi, anti-CD200RAutoimmunity via NKG2D + CD8 T-cells; IP collapse; new therapies
39021583 [71]Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives Li YComput Struct Biotechnol J2024Review (multi-omics)AGA patient datasetsMulti-omics integrationOmics reveal AGA mechanisms; biomarkers identified
11703920 [72]At the roots of a never-ending cycle Fuchs EDev Cell2001Review Bulge stem cells orchestrate hair cycle; Wnt/BMP regulation
16901790 [73]Blimp1 defines a progenitor population that governs epidermal seal formation and hair follicle morphogenesisHorsley VCell2006Genetic knockoutLaboratorySebaceous progenitorsBlimp1 deletionSebaceous hyperplasia
15024388 [74]Capturing and profiling adult hair follicle stem cells Morris RJNat Biotechnol2004FACS isolation + profilingMouse dorsal skinK15+ bulge cellsTamoxifen-inducible Cre, microarrayK15+ SCs reconstitute epidermis/HF/SG; high proliferative
19629164 [75]Circadian clock genes contribute to the regulation of hair follicle cyclingLin KKPLoS Genet2009Genomics/mutant analysisMouse skin (C57BL/6)Telogen/early anagen HFsGene expression profilingClock genes delay anagen via cell cycle (p21 up, Rb hypophospho)
25210331 [76]Classification Framework for Healthy Hairs and Alopecia Areata: A Machine Learning (ML) ApproachShakeel CSComputational and Mathematical Methods in Medicine2021Machine learning classification studySingle-center; image datasetsClinically diagnosed healthy scalps vs. alopecia areata casesML algorithms (SVM, KNN, etc.) for trichoscopic image classificationML framework achieved high accuracy (up to 98%) distinguishing healthy hair from alopecia areata
11152763 [2]Controls of hair follicle cycling Stenn KSPhysiol Rev2001ReviewN/A (integrates mouse/human models) Epithelial-mesenchymal interactions control cycle; FGF/TGF-β/Wnt/Shh
12015981 [77]Coordinated transcription of key pathways in the mouse by the circadian clock Panda SCell2002Microarray time-seriesMouse liver/SCNWildtype SCN/liver tissuesCircadian sampling (24 h)~650 cycling transcripts; clock coordinates metabolism
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36286377 [40]Hair Follicle Classification and Hair Loss Severity Estimation Using Mask R-CNNKim JHJ Imaging2022Deep learning modelDermoscopic imagesHealthy/normal/severe HF imagesMask R-CNN (ResNet backbone)92% accuracy HF classification; severity index Pavg via heatmap
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33062040 [39]Trichoscopy of Alopecia Areata: Hair Loss Feature Extraction and Computation Using Grid Line Selection and Eigenvalue pmc.ncbi.nlm.nihSeo SComput Math Methods Med2020Algorithm development/evaluationDermoscopy scalp imagesAlopecia areata scalp images (N = NR)Scalp images with microscope/smartphoneGrid line selection + eigenvalue for HLF (hair count, follicle, thickness)
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10805917 [85]Intercellular junctions between palisade nerve endings and outer root sheath cells of rat vellus hairsKaidoh TJournal of Comparative Neurology2000Electron microscopy ultrastructural studyLaboratoryPalisade nerve endings (PNs) associated with vellus hair outer root sheath (ORS) cellsTransmission electron microscopy to examine junctional structures between PNs and ORSPNs form close membrane appositions and adherens-like junctions with ORS cells, suggesting bidirectional signaling between nerve and follicle
10966107 [86]Involvement of follicular stem cells in forming not only the follicle but also the epidermisTaylor GCell2000Experimental (labeling/tracing)Mouse skin (newborn/adult)Mice (unspecified N)Normal/wounded mouse skinDouble-label technique for keratinocyte migration
2364430 [87]Label-retaining cells reside in the bulge area of pilosebaceous unit: implications for follicular stem cells, hair cycle, and skin carcinogenesisCotsarelis GCell1990BrdU label-retainingMouse epidermisBasal keratinocytesContinuous BrdU + TPABulge LRCs = quiescent stem cells; activated by TPA
38545843 [38]Leveraging deep neural networks to uncover unprecedented levels of precision in the diagnosis of hair and scalp disordersChowdhury MSSkin Res Technol2024Deep learning modelDermoscopy datasetHair/scalp disordersXception CNN + attention92.5% accuracy, superior to dermatologists in classification
10899998 [27]Modeling the dynamics of human hair cycles by a follicular automatonHalloy JPNAS2000Computational modelSimulation (human scalp)Alopecic/non-alopecic dataStochastic automaton rulesModel reprudicing alopecia pattern
15714560 [88]Molecular principles of hair follicle induction and morphogenesisSchmidt-Ullrich RBioessays2005Review Activator-inhibitor gradients drive placode/condensate pmc.ncbi.nlm.nih
11207364 [89]Morphogenesis and renewal of hair follicles from adult multipotent stem cellsOshima HCell2001Experimental transplantationLaboratory (mouse)Multipotent stem cells from upper ORSFollicle transplantation assaysAdult stem cells regenerate complete follicle structures and epidermis
25398054 [90]Characterization of quiescent epithelial cells in mouse meibomian glands and hair follicle/sebaceous glands by immunofluorescence tomographyGeraint J ParfittJ Invest Dermatol2015Experimental (immunofluorescence tomography)Mouse eyelids (meibomian glands, hair follicle/sebaceous glands)Mice (N not specified)H2B-GFP label-retaining cells (LRCs) in glandsImmunofluorescence tomography with markers (Sox9, Blimp1, PPARγ)
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20798039 [31]Noninvasive method for assessing the human circadian clock using hair follicle cellsAkashi MProceedings of the National Academy of Sciences of the USA2010Experimental/translational studySingle-center laboratory; volunteersHealthy individuals with regular sleep–wake schedules providing serial hair samplesNoninvasive sampling of hair follicles followed by clock-gene expression analysis ex vivoCircadian phase and period can be estimated from hair-follicle clock-gene rhythms, providing a practical tool to assess human circadian timing
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33573119 [92]Hair Histology and Glycosaminoglycans Distribution Probed by Infrared Spectral Imaging: Focus on Heparan Sulfate Proteoglycan and Glypican-1 during Hair Growth CycleCharlie Colin-PierreBiomolecules2021Experimental (IR spectral imaging, IHC, WB)Human hair folliclesHuman HF sections (32 anagen, 28 catagen, 31 telogen from 4 donors)HFs at anagen/catagen/telogen phasesInfrared spectral imaging for sulfated GAGs/HSPGs; IHC/WB for glypican-1
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7487740 [94]Quantification of hair follicle parameters using computer image analysis: a comparison of androgenetic alopecia with normal scalp biopsiesLee MSAustralas J Dermatol1995Quantitative histology/image analysisHorizontal scalp biopsiesAGA patients (10) + controls (10)Histologically confirmed AGA/normal scalpAGA: ↓ follicle diameter (236 vs. 268 μm), ↓ T:V ratio (3:1 vs. 36:1), ↓ ORS area
35726958 [34]Quantitative characterization of 3D structure of vellus hair arrector pili muscles by micro CTEzure TSkin Research and Technology2022Micro-CT imagingLaboratoryVellus arrector pili3D reconstructionDetailed muscle geometry quantified
25410793 [95]Resting no more: re-defining telogen, the maintenance stage of the hair growth cycleGeyfman MBiol Rev Camb Philos Soc2015Review Telogen = active maintenance; sub-stages refractory/competent
21753860 [96]Steady and temporary expressions of smooth muscle actin in hair, vibrissa, arrector pili muscle, and other hair appendages of developing ratsMorioka KActa Histochemica et Cytochemica2011Developmental IHCLaboratoryHair appendagesSMA immunostainingStage-specific expression patterns
10441606 [97]The Biology of Hair FolliclesPaus RNew England Journal of Medicine1999Review Follicle biologyDynamic mini-organ concept
34535902 [98]The circadian clock and diseases of the skinDuan JFEBS Lett2021Review Circadian disruption linked to alopecia, psoriasis; clock genes in HF cycling
20590819 [1]The cycling hair follicle as an ideal systems biology research modelAl-Nuaimi YExp Dermatol2010Review/model proposalN/A (model discussion)N/A (human/mouse HF)Cycling mammalian HFsHF as mini-organ model for systems biology/chronobiology; translational potential
35962707 [36]The Emergent Power of Human Cellular vs. Mouse Models of Hair Follicle RegenerationCastro ARStem Cells Translational Medicine2022Narrative reviewNot applicable (review)Compares human vs. mouse hair biology and models for regeneration studiesNot applicable (review)Human cellular models superior to mouse for translational hair loss research due to anatomical and cycling differences
19183169 [99]How not to get scar(r)ed: pointers to the correct diagnosis in patients with suspected primary cicatricial alopeciaHarries MJBr J Dermatol2009ReviewClinical (human patients)Patients with suspected PCAClinical/histopath features of PCAPrimary cicatricial alopecias are rare (~3–7%) disorders causing irreversible hair loss, requiring early but challenging diagnosis
19211055 [100]The hair follicle as a dynamic miniorganSchneider MRCurr Biol2009ReviewNot applicable (review)Reviews structure, cycling, and signaling pathways of the hair follicle as a mini-organNot applicable (review)Summarizes key molecular and cellular mechanisms underlying hair follicle morphogenesis, cycling, and disorders
28266743 [101]The hair follicle enigmaBernard BAExperimental Dermatology2017Narrative reviewNot applicable (review)Review of hair follicle structure, cycling, and unsolved biological questionsNot applicable (review)Highlights key enigmas in hair follicle biology including glycobiology, exosomes and translational gaps
24952302 [102]Three-dimensional reconstruction of light microscopy image sections: present and futureWang YFrontiers in Medicine2014Review (3D methods)Histological sectionsLight microscopy sectionsSerial sectioning + software alignment3D reconstruction reveals HF microstructures
25822259 [103]Thyroxine differentially modulates the peripheral clock: lessons from the human hair follicleVidali SPLoS One2015Ex vivo organ cultureHuman HF cultureAnagen scalp HFs from surgeryT4 (100 nM), light/dark cycleT4 alters clock gene expression in HFs
26476248 [104]Selected Disorders of Skin Appendages—Acne, Alopecia, HyperhidrosisVary JC JrMed Clin North Am2015ReviewN/AN/AAcne, alopecia, hyperhidrosis casesSelected Disorders of Skin Appendages—Acne, Alopecia, Hyperhidrosis
12756226 [28]Transient activation of beta-catenin signaling in cutaneous keratinocytes is sufficient to trigger the active growth phase of the hair cycle in miceVan Mater DGenes & Development2003Experimental transgenicLaboratoryAdult telogen skinTamoxifen-induced beta-catenin activationInduces anagen hair growth
30951234 [105]Understanding skin morphogenesis across developmental, regenerative, and evolutionary levelsPlikus MVExp Dermatol2019Editorial/review Morphogenesis insights from evolution/regeneration for skin appendages
9238319 [106]Whole hair follicle culture Philpott MPDermatol Clin1996Review/protocolEx vivoIntact HFs for cultureSerum-free medium (William’s E)HF culture protocol
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Key studies were selected based on their central role within the pruned citation network, representing methodological hubs or thematic bridges across communities. Most studies were experimental or diagnostic in nature, with limited reporting of sample size and follow-up duration, reflecting the exploratory and technology-driven focus of the field.

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Figure 1. PRISMA flow diagram. Study selection process from MEDLINE/PubMed search (n = 1261) to included studies (n = 58), including citation-network pruning (n = 1203 excluded). * Records were identified through MEDLINE/PubMed database searches only; no registers were used. ** Records were excluded during citation-network pruning because they showed low connectivity within the network or were isolated nodes, and therefore not part of the main citation structure.
Figure 1. PRISMA flow diagram. Study selection process from MEDLINE/PubMed search (n = 1261) to included studies (n = 58), including citation-network pruning (n = 1203 excluded). * Records were identified through MEDLINE/PubMed database searches only; no registers were used. ** Records were excluded during citation-network pruning because they showed low connectivity within the network or were isolated nodes, and therefore not part of the main citation structure.
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Figure 2. Thematic network map of included studies: a pruned keyword co-occurrence network depicting the main thematic clusters identified in the literature. Nodes represent keywords, edges indicate co-occurrence relationships, and colored hulls highlight community structure (topic clusters), including circadian/clock proteins, smooth muscle biology, murine cell/protein studies, dermatology–hair follicle research, neural networks/hair, and animal cell-related themes.
Figure 2. Thematic network map of included studies: a pruned keyword co-occurrence network depicting the main thematic clusters identified in the literature. Nodes represent keywords, edges indicate co-occurrence relationships, and colored hulls highlight community structure (topic clusters), including circadian/clock proteins, smooth muscle biology, murine cell/protein studies, dermatology–hair follicle research, neural networks/hair, and animal cell-related themes.
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Figure 3. Exemplificative heatmap of aggregated hair loss severity across the scalp. Follicle-level parameters are spatially integrated to generate a local severity index (P_avg), visualized as a color-coded heatmap. The figure is schematic and intended for illustrative purposes only.
Figure 3. Exemplificative heatmap of aggregated hair loss severity across the scalp. Follicle-level parameters are spatially integrated to generate a local severity index (P_avg), visualized as a color-coded heatmap. The figure is schematic and intended for illustrative purposes only.
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Table 1. Overview of artificial intelligence–based studies for trichoscopic and scalp image analysis in hair and scalp disorders, summarizing study design, database characteristics, data source, reported outcomes, and availability of comparative evaluations.
Table 1. Overview of artificial intelligence–based studies for trichoscopic and scalp image analysis in hair and scalp disorders, summarizing study design, database characteristics, data source, reported outcomes, and availability of comparative evaluations.
StudyYearTypeNumerosity of DBDB SourceReported OutcomesComparative Data AvailableValues
Kim M. et al.—Evaluation of Automated Measurement of Hair Density Using Deep Neural Networks (10.3390/s22020650) [37]2022Retrospective AI validation study4492 images; 817 patientsNational Information Society Agency (Korea) dataset; restricted to Korean male cohortMean Average Precision (mAP) for follicle detectionYes—comparison among YOLOv4, EfficientDet, DetectoRSYOLOv4: 58.67% mAP (highest)
Seo S. and Park J.—Trichoscopy of Alopecia Areata: Hair Loss Feature Extraction
and Computation Using Grid Line Selection and Eigenvalue (10.1155/2020/6908018) [39]
2020Retrospective AI validation study100n-house scalp microscopy images captured with Galaxy Tab S4 + microscope (20×–800×; two microscope types)Hair feature extraction (HLF): hair count, follicle count, hair thickness; accuracy reportedNoMean accuracy: 96.51%; Table 1 (mean): hair truth 19.59 vs. pred 19.04 (diff 3.13); follicle truth 8.15 vs. pred 8.49 (diff 1.44); mean thickness pred 61.98; max error: hair 16, follicle 4.
Kim JH. et al.—Hair Follicle Classification and Hair Loss Severity Estimation Using Mask R-CNN (10.3390/jimaging8100283) [40]2022Retrospective AI development/validation study600 RGB images; 10 male subjectsProprietary acquisition (microscopic scalp imaging)Follicle instance segmentation + follicle status classification + severity heatmapNo head-to-head model comparison reported as primary aimTrain/test split reported (450/150); performance metrics reported in paper
Gao M. et al.—Deep Learning-based Trichoscopic Image Analysis and Quantitative Model for Predicting Basic and Specific Classification in Male Androgenetic Alopecia (10.2340/actadv.v101.564) [41]2022Retrospective AI framework + predictive model2910 trichoscopic images; 582 subjects (528 AGA + 54 controls)Proprietary clinical dataset; no shavingAutomated hair density + diameter distribution extraction; BASP prediction modelPartially (internal model comparisons/variants)Dataset split reported (2310 train/300 val/300 test; no participant overlap)
Di Fraia M. et al.—A Machine Learning Algorithm Applied to Trichoscopy for AGA Severity Assessment (10.5826/dpc.1303a136) [42]2023Retrospective ML studyN images: NR; 200 patients (100 M, 100 F)Proprietary outpatient cohort; Trichoscale Pro®-based parametersMild vs. moderate–severe AGA classification + severity probability indexNoAccuracy: 94.3% (train), 90.0% (test); AUC: 0.99 (train), 0.95 (test)
Suh MJ. et al.—Automated Early Detection of Androgenetic Alopecia Using Deep Learning on Trichoscopic Images from a Korean Cohort (10.12771/emj.2025.00486) [43]2025Retrospective DL model development/validation318 trichoscopic scalp images; N patients: NREwha Womans University Medical Center; dataset not shared (privacy)Binary classification: BASP 0 vs. BASP 1–3 (early AGA)NoModel: ResNet-18 (ImageNet pretrained), fine-tuned; class distribution 159 vs. 159
Table 2. Proof-of-concept studies and currently available AI-assisted trichoscopy platforms, summarizing system type, datasets, validation methods, and reported outcomes. Academic systems demonstrate the feasibility of automated hair morphometric analysis, while commercial platforms extend these approaches to real-time, smartphone-based scalp assessment, often relying on proprietary datasets and non-public validation.
Table 2. Proof-of-concept studies and currently available AI-assisted trichoscopy platforms, summarizing system type, datasets, validation methods, and reported outcomes. Academic systems demonstrate the feasibility of automated hair morphometric analysis, while commercial platforms extend these approaches to real-time, smartphone-based scalp assessment, often relying on proprietary datasets and non-public validation.
Study (PMID)SystemDOI/LinkYearTypeDeveloper/ManufacturerDataset/Sample SizeGround Truth/ValidationReported OutcomesData Available
A novel automated approach to rapid and precise in vivo measurement of hair morphometrics using a smartphone (34251055) [44]NR10.1111/srt.130762021Portable Dermoscope + laptop + Matlab® 50 patientsManual expert countingAutomatic: 24 s, manual: 9.2 min; equivalent within 20% (density/diameter) on 50 scalps (p < 0.001 correlation)Yes
Development and qualification of a machine learning algorithm for automated hair counting (34426987) [19]HairMetrix®10.1111/ics.127352021AI/ML phototrichogram analysis (deep CNN)Procter & Gamble + Canfield Scientific (Fairfield, NJ, USA)288 manually annotated phototrichogram images (hair location/length)Semi-manual Canfield HairMetrix; high reproducibility agreementAutomated count/length in seconds (vs. months manual); 100× cost/time reductionYes
Consumer app (no PMID)Hair AI Scanner https://apps.apple.com/it/app/hair-ai-hair-scanner-care/id6749930117 (accessed on 20 March 2026)2025Smartphone AI scannerDO Mai Ly/AIanyNR (proprietary)NR (no clinical validation)Density/porosity/thickness/split ends/scalp health; personalized plansNo
Consumer app (No PMID)HairLens AI https://hairlensai.com/ (accessed on 20 March 2026)2025Smartphone AI multi-angle hair/scalp scannerUsman Yousaf170,000+ clinical images from 12 international centersNo published clinical validation (claims 94% diagnostic accuracy, 95% expert correlation)Regional density (170 hairs/cm2), growth phases (85% anagen), treatment matching (FUE 98%, PRP 85%), health scoresNo
Medical Device (no PMID)Trichoschale®/TrichoLAB®/skeen (FotoFinder Ecosystem;)https://www.tricholab.com/ (accessed on 20 March 2026)2023–20243D imaging + cloud analyticsFotoFinder Systems (Warsaw, Poland)Proprietary (commercial)Manual + software metrics; internal QAHair density, shaft diameter, empty follicle detectionNo
Medical Device (No PMID)CASLite Nova https://www.catseyetech.in/caslite.html (accessed on 20 March 2026)2016 Cats Eye Systems & Solutions Pvt. Ltd. (Mumbai, India) Claims: density, thickness, alopecia typeNo
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Zengarini, C.; Curti, N.; Cedirian, S.; Rapparini, L.; Pampaloni, F.; Pileri, A.; Durazzi, F.; Mussi, M.; La Placa, M.; Piraccini, B.M.; et al. Trichoscopy and Computational Models for Hair and Scalp Disorders: Image Analysis, Quantification, and Clinical Integration. Appl. Sci. 2026, 16, 3199. https://doi.org/10.3390/app16073199

AMA Style

Zengarini C, Curti N, Cedirian S, Rapparini L, Pampaloni F, Pileri A, Durazzi F, Mussi M, La Placa M, Piraccini BM, et al. Trichoscopy and Computational Models for Hair and Scalp Disorders: Image Analysis, Quantification, and Clinical Integration. Applied Sciences. 2026; 16(7):3199. https://doi.org/10.3390/app16073199

Chicago/Turabian Style

Zengarini, Corrado, Nico Curti, Stephano Cedirian, Luca Rapparini, Francesca Pampaloni, Alessandro Pileri, Francesco Durazzi, Martina Mussi, Michelangelo La Placa, Bianca Maria Piraccini, and et al. 2026. "Trichoscopy and Computational Models for Hair and Scalp Disorders: Image Analysis, Quantification, and Clinical Integration" Applied Sciences 16, no. 7: 3199. https://doi.org/10.3390/app16073199

APA Style

Zengarini, C., Curti, N., Cedirian, S., Rapparini, L., Pampaloni, F., Pileri, A., Durazzi, F., Mussi, M., La Placa, M., Piraccini, B. M., & Starace, M. (2026). Trichoscopy and Computational Models for Hair and Scalp Disorders: Image Analysis, Quantification, and Clinical Integration. Applied Sciences, 16(7), 3199. https://doi.org/10.3390/app16073199

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