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Marshall syndrome
Medical condition / From Wikipedia, the free encyclopedia
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Marshall syndrome is a genetic disorder of the connective tissue[2] that can cause hearing loss. The three most common areas to be affected are the eyes, which are uncommonly large, joints and the mouth and facial structures. Marshall syndrome and Stickler syndrome closely resemble each other; in fact they are so similar, some say they are the same.[3][4] The condition is named for D. Weber.[5]
Quick Facts Other names ...
Marshall syndrome | |
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Other names | Deafness, myopia, cataract, saddle nose-Marshall type [1] |
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Marshall syndrome and Stickler syndrome is inherited in an autosomal dominant pattern. |
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