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Cardiogenetics, Volume 11, Issue 1

2021 March - 5 articles

Cover Story: Cardiac amyloidosis is the result of extracellular deposition of amyloid fibrils throughout the heart. Treatment success mostly depends on early diagnosis for AL amyloidosis, while for ATTR amyloidosis, new investigational agents are being studied that can reduce production of transthyretin protein. This review aimed to investigate the current understanding and new research on cardiac amyloidosis new treatment strategies and their clinical outcome. View this paper

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Articles (5)

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Case Report

1 Citations

4,453 Views

8 Pages

Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report

Sigita Glaveckaitė,
Violeta Mikštienė,
Eglė Preikšaitienė,
Rimvydas Norvilas,
Ramūnas Janavičius and
Nomeda Rima Valevičienė

Cardiogenetics2021, 11(1), 31-38;https://doi.org/10.3390/cardiogenetics11010005

5 March 2021

Hypertrophic cardiomyopathy and left ventricular noncompaction commonly occur as separate disorders with distinct clinical and pathoanatomical features. However, these cardiomyopathies may have a similar genetic origin with mutations encoding sarcome...

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Editorial

2 Citations

3,520 Views

3 Pages

Genetic Susceptibility to SARS-CoV-2: From the Nehandertal Age to 2020

Federica Amodio,
Martina Caiazza,
Paolo Calabrò and
Giuseppe Limongelli

Cardiogenetics2021, 11(1), 28-30;https://doi.org/10.3390/cardiogenetics11010004

25 February 2021

Since late 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its associated coronavirus disease 2019 (COVID-19) have become a worldwide threat to public health [...]

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Case Report

1 Citations

4,750 Views

10 Pages

Three Myocardial Diseases in One Heart: Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Noncompaction and Myocarditis

Yulia Lutokhina,
Olga Blagova,
Nadezhda Varionchik,
Svetlana Alexandrova,
Nina Gagarina,
Eugenia Kogan,
Vsevolod Sedov,
Anna Shestak,
Elena Zaklyazminskaya and
Alexander Nedostup

Cardiogenetics2021, 11(1), 18-27;https://doi.org/10.3390/cardiogenetics11010003

10 February 2021

Purpose: To evaluate the clinical features, laboratory and instrumental tests results and the effectiveness of complex treatment in a patient with multiple etiologies of dilated cardiomyopathy (DCM) with a high risk of sudden cardiac death. Methods:...

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Communication

2 Citations

6,781 Views

8 Pages

Cardiac Amyloidosis Therapy: A Systematic Review

Franco Iodice,
Marco Di Mauro,
Marco Giuseppe Migliaccio,
Angela Iannuzzi,
Roberta Pacileo,
Martina Caiazza and
Augusto Esposito

Cardiogenetics2021, 11(1), 10-17;https://doi.org/10.3390/cardiogenetics11010002

31 January 2021

Heart involvement in Cardiac Amyloidosis (CA) results in a worsening of the prognosis in almost all patients with both light-chain (AL) and transthyretin amyloidosis (ATTR). The mainstream CA is a restrictive cardiomyopathy with hypertrophic phenotyp...

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Case Report

8 Citations

5,250 Views

9 Pages

Mosaic Fabry Disease in a Male Presenting as Hypertrophic Cardiomyopathy

Maria Xu,
Christopher Orsborne,
James Eden,
Andrew Wallace,
Heather J. Church,
Karen Tylee,
Sasalu Deepak,
Christopher Cassidy,
Peter Woolfson and
William G. Newman
+ 3 authors

Cardiogenetics2021, 11(1), 1-9;https://doi.org/10.3390/cardiogenetics11010001

31 December 2020

We describe a 55 year old male diagnosed with cardiomyopathy due to Fabry disease. Biochemical testing of blood spot and plasma showed low-normal alpha-galactosidase A (α-Gal A) levels. Genetic testing revealed somatic mosaicism for GLA c.901C&...

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Cardiogenetics - ISSN 2035-8148

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