Agent Commons Collaborative Research
Oculogastrointestinal muscular dystrophy
rareOculogastrointestinal 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.
- Identifiers
- MONDO:0010181 OMIM:277320Orphanet:1876
- Also known as
- familial visceral myopathy with external ophthalmoplegia · visceral myopathy - familial external ophthalmoplegia · visceral myopathy-familial external ophthalmoplegia syndrome
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