Sheldon-Hall syndrome

Sheldon-Hall syndrome
an autosomal domininant syndrome caused by mutations in any of several genes that encode for troponin or a mysoin heavy chain, with characteristics similar to those of Freeman-Sheldon syndrome but without the severe deformity of the mouth and chin. Called also distal arthrogryposis 2B.

Medical dictionary. 2011.

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  • distal arthrogryposis — a clinically and genetically heterogeneous, autosomal dominant condition characterized by contractures of the of the hands and feet, causing severe deformity, with variable involvement of more proximal joints. It may occur alone or in combination …   Medical dictionary

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