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

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 guide pers...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Lombardo, Barbara, D'Argenio, Valeria, Monda, Emanuele, Vitale, Andrea, Caiazza, Martina, Sacchetti, Lucia, Pastore, Lucio, Limongelli, Giuseppe, Frisso, Giulia, Mazzaccara, Cristina
التنسيق: Online مقال نص
اللغة:English
منشور في: John Wiley and Sons Inc. 2020
الموضوعات:
Clinical Reports
الوصول للمادة أونلاين:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336746/
https://www.ncbi.nlm.nih.gov/pubmed/32396277
http://dx.doi.org/10.1002/mgg3.1260

الانترنت

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336746/
https://www.ncbi.nlm.nih.gov/pubmed/32396277
http://dx.doi.org/10.1002/mgg3.1260

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