Synonyms: Distal arthrogryposis type 7 | Dutch-Kentucky syndrome | Hecht syndrome | Hecht-Beals syndrome
A rare genetic distal arthrogryposis characterized by pseudocamptodactyly mild foot deformities moderately short stature and short muscles and tendons resulting in a limited range of motion of the hands legs and mouth the later presenting with trismus.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
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