Clinico-pathological diagnosis of Facioscapulohumeral Dystrophy in a 22-year-old Male

Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2.03–6.8 per 100,000 individuals. FSHD is the third most common type of muscular dystrophy after the Duchene muscular dystrophy and myotonic dystrophy. To the best of our knowledge, the current case re...

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Bibliographic Details
Main Authors: Biniyam A. Ayele, Riyad Ibrahim, Keberte Tsegaye, Tadele Birhanu, Hanna Assefa, Wondwossen Ergete
Format: Article
Language:English
Published: Knowledge E 2021-03-01
Series:Sudan Journal of Medical Sciences
Subjects:
Online Access:https://doi.org/10.18502/sjms.v16i1.8945