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Article

Retinal Changes in Early-Onset cblC Methylmalonic Acidemia Identified Through Expanded Newborn Screening: Highlights from a Case Study and Literature Review

Institute for Maternal and Child Health “Burlo Garofolo”, 34137 Trieste, TS, Italy
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Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Genes 2025, 16(6), 635; https://doi.org/10.3390/genes16060635
Submission received: 19 April 2025 / Revised: 23 May 2025 / Accepted: 24 May 2025 / Published: 25 May 2025
(This article belongs to the Section Molecular Genetics and Genomics)

Abstract

Background: Methylmalonic acidemia combined with homocystinuria (cblC) can lead to infantile maculopathy. Although significant visual deterioration is commonly reported in early-onset cblC, we found poor awareness regarding formal assessments of ocular complications, especially in newborns, and of how these complications relate to the timing of therapy initiation. In this work, we present our experience and perform a literature review. Methods: We performed sequential fundus examinations, optical coherence tomography (OCT) and full-field electroretinography (ERG) under sedation following detection of signs of retinal degeneration. We also assessed visual fields using kinetic attraction perimetry. Results: We report a newborn who was referred on the eighth day of life, following a diagnosis of cblC through newborn screening (NBS), and who began treatment that same day. Close monitoring of retinal changes through fundus examinations allowed the detection of signs of retinal degeneration at 3 months, which progressed when checked at 5 months. At 7 months, OCT showed retinal thinning with the appearance of bull’s eye maculopathy in the corresponding region on fundoscopy; ERG revealed a reduction in the amplitude of both scotopic and photopic components, whereas kinetic attraction perimetry showed no abnormalities. Genetic investigation confirmed the disease, compound heterozygous for a nonsense variant in MMACHC and a splicing one in PRDX1. Conclusions: In cblC, retinal degeneration occurs in the first months of life despite timely treatment and adequate biochemical control, and it may manifest before any signs of visual deprivation appear. However, there is an early, narrow window during which therapy may slow down retinal degeneration enough to prevent sensory nystagmus. We recommend initiating therapy immediately after biochemical diagnosis, along with close ophthalmological monitoring, before the appearance of any signs.
Keywords: tandem mass spectrometry biomarkers; epi-cblC; infantile maculopathy; BEM; sensory nystagmus; motor nystagmus tandem mass spectrometry biomarkers; epi-cblC; infantile maculopathy; BEM; sensory nystagmus; motor nystagmus

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MDPI and ACS Style

Michieletto, P.; Baldo, F.; Madonia, M.; Zupin, L.; Pensiero, S.; Bonati, M.T. Retinal Changes in Early-Onset cblC Methylmalonic Acidemia Identified Through Expanded Newborn Screening: Highlights from a Case Study and Literature Review. Genes 2025, 16, 635. https://doi.org/10.3390/genes16060635

AMA Style

Michieletto P, Baldo F, Madonia M, Zupin L, Pensiero S, Bonati MT. Retinal Changes in Early-Onset cblC Methylmalonic Acidemia Identified Through Expanded Newborn Screening: Highlights from a Case Study and Literature Review. Genes. 2025; 16(6):635. https://doi.org/10.3390/genes16060635

Chicago/Turabian Style

Michieletto, Paola, Francesco Baldo, Maurizio Madonia, Luisa Zupin, Stefano Pensiero, and Maria Teresa Bonati. 2025. "Retinal Changes in Early-Onset cblC Methylmalonic Acidemia Identified Through Expanded Newborn Screening: Highlights from a Case Study and Literature Review" Genes 16, no. 6: 635. https://doi.org/10.3390/genes16060635

APA Style

Michieletto, P., Baldo, F., Madonia, M., Zupin, L., Pensiero, S., & Bonati, M. T. (2025). Retinal Changes in Early-Onset cblC Methylmalonic Acidemia Identified Through Expanded Newborn Screening: Highlights from a Case Study and Literature Review. Genes, 16(6), 635. https://doi.org/10.3390/genes16060635

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