Oculogastrointestinal muscular dystrophy

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.

Also known as: visceral myopathy-familial external ophthalmoplegia syndrome, familial visceral myopathy with external ophthalmoplegia, intestinal pseudoobstruction with external ophthalmoplegia, muscular dystrophy, oculogastrointestinal, visceral myopathy - familial external ophthalmoplegia, visceral myopathy, familial, with external ophthalmoplegia

3 clinical trials for this condition and its sub-types, 0 tagged with Oculogastrointestinal muscular dystrophy itself.