Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: a case report

BACKGROUND: Danon disease (OMIM 300257) is an X-linked lysosomal storage disorder, characterized by hypertrophic cardiomyopathy (HCM), skeletal myopathy, variable intellectual disability, and other minor clinical features. This condition accounts for ~ 4% of HCM patients, with a more severe and earl...

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Detalles Bibliográficos
Autores principales: Novelli, Valeria, Bisignani, Antonio, Pelargonio, Gemma, Primiano, Guido, Narducci, Maria Lucia, Palmieri, Vincenzo, Tiziano, Francesco Danilo, Zeppilli, Paolo, Servidei, Serenella, Crea, Filippo, Genuardi, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132987/
https://www.ncbi.nlm.nih.gov/pubmed/32248794
http://dx.doi.org/10.1186/s12872-020-01421-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132987/
https://www.ncbi.nlm.nih.gov/pubmed/32248794
http://dx.doi.org/10.1186/s12872-020-01421-4

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