A case of type 1 facioscapulohumeral muscular dystrophy (FSHD) with restrictive ventilatory defect and congestive heart failure
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DOI: 10.1016/j.ensci.2020.100284
Abstract: [Background] Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscle disease characterized by asymmetric involvement of muscles in the face, upper extremity, trunk, and lower extremity regions, with variable severity. It was recently reported that… read more here.
Keywords: dystrophy fshd; muscular dystrophy; facioscapulohumeral muscular; restrictive ventilatory ... See more keywords