Familial visceral myopathy with external ophthalmoplegia
Other Names: Oculogastrointestinal muscular dystrophy; Muscular dystrophy, oculogastrointestinal; Intestinal pseudoobstruction with external ophthalmoplegia; Visceral myopathy, familial, with external ophthalmoplegia; Visceral myopathy - familial external ophthalmoplegia
Oculogastrointestinal muscular dystrophy is an extremely rare autosomal recessively inherited neuromuscular disease characterized by ocular manifestations such as ptosis and diplopia followed by chronic diarrhea, malnutrion and intestinal peudo-obstruction.
NIH genetic and rare disease info[edit source]
Familial visceral myopathy with external ophthalmoplegia is a rare disease.
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