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Results 1 - 1 of 1 for Facioscapulohumeral muscular dystrophy 2
  1. Chromosome 4 
    ... of the usual 11 to 100 repeats. In facioscapulohumeral muscular dystrophy type 2 (FSHD2), hypomethylation is most often a result of ... may have two "permissive" copies of chromosome 4, two "non-permissive" copies, or one of each. Facioscapulohumeral muscular dystrophy can only occur in people who have at ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics