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A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome

We report a case of a five-month-old girl, who presented to our hospital with increased work of breathing, sweating since birth, and abnormal eye movements. On further evaluation, she was found to have restrictive cardiomyopathy, nystagmus, and hypotonia. Genetic workup showed a pathogenic variant i...

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Detalles Bibliográficos
Autores principales: Snobar, Rania, Mohamed, Madiha, AlKamali, Ahmed, Gupta, Bhavna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867829/
https://www.ncbi.nlm.nih.gov/pubmed/36694529
http://dx.doi.org/10.7759/cureus.32857
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author Snobar, Rania
Mohamed, Madiha
AlKamali, Ahmed
Gupta, Bhavna
author_facet Snobar, Rania
Mohamed, Madiha
AlKamali, Ahmed
Gupta, Bhavna
author_sort Snobar, Rania
collection PubMed
description We report a case of a five-month-old girl, who presented to our hospital with increased work of breathing, sweating since birth, and abnormal eye movements. On further evaluation, she was found to have restrictive cardiomyopathy, nystagmus, and hypotonia. Genetic workup showed a pathogenic variant in the ALSM1 gene, which confirmed the diagnosis of Alström syndrome. Alström syndrome is a rare condition that is characterized by a wide variety of multisystem manifestations, including visual disturbances, hearing impairment, and cardiomyopathy. This case report highlights Alström syndrome as one of the rare causes of early-onset infantile cardiomyopathy with nystagmus.
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spelling pubmed-98678292023-01-23 A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome Snobar, Rania Mohamed, Madiha AlKamali, Ahmed Gupta, Bhavna Cureus Cardiology We report a case of a five-month-old girl, who presented to our hospital with increased work of breathing, sweating since birth, and abnormal eye movements. On further evaluation, she was found to have restrictive cardiomyopathy, nystagmus, and hypotonia. Genetic workup showed a pathogenic variant in the ALSM1 gene, which confirmed the diagnosis of Alström syndrome. Alström syndrome is a rare condition that is characterized by a wide variety of multisystem manifestations, including visual disturbances, hearing impairment, and cardiomyopathy. This case report highlights Alström syndrome as one of the rare causes of early-onset infantile cardiomyopathy with nystagmus. Cureus 2022-12-23 /pmc/articles/PMC9867829/ /pubmed/36694529 http://dx.doi.org/10.7759/cureus.32857 Text en Copyright © 2022, Snobar et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Cardiology
Snobar, Rania
Mohamed, Madiha
AlKamali, Ahmed
Gupta, Bhavna
A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome
title A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome
title_full A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome
title_fullStr A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome
title_full_unstemmed A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome
title_short A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome
title_sort rare cause of infantile-onset cardiomyopathy with ocular manifestations: alström syndrome
topic Cardiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867829/
https://www.ncbi.nlm.nih.gov/pubmed/36694529
http://dx.doi.org/10.7759/cureus.32857
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