Facioscapulohumeral Muscular Dystrophy Type 2

About the Disease
Facioscapulohumeral Muscular Dystrophy 2, Digenic, also known as facioscapulohumeral muscular dystrophy 2, is related to neuromuscular disease and muscular dystrophy. An important gene associated with Facioscapulohumeral Muscular Dystrophy 2, Digenic is SMCHD1 (Structural Maintenance Of Chromosomes Flexible Hinge Domain Containing 1). The drug Creatine has been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and lung, and related phenotypes are facial palsy and hearing impairment

Common Targets
DUX4L1 | SMCHD1

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