Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome

Abstract Background Syndromic dilated cardiomyopathy (DCM) includes a group of complex disorders with a very heterogeneous genetic etiology, leading to delay in definitive diagnosis. Conversely, an early genetic diagnosis is very important in determining the disease course, the prognosis, and may gu...

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Autores principales:	Barbara Lombardo, Valeria D'Argenio, Emanuele Monda, Andrea Vitale, Martina Caiazza, Lucia Sacchetti, Lucio Pastore, Giuseppe Limongelli, Giulia Frisso, Cristina Mazzaccara
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Wiley 2020-07-01
Colección:	Molecular Genetics & Genomic Medicine
Materias:	Alström syndrome array CGH idiopathic cardiomyopathy mitochondrial syndromic dilated cardiomyopathy Usher syndrome
Acceso en línea:	https://doi.org/10.1002/mgg3.1260
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