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Trismus-pseudocamptodactyly syndrome

Disease Export to PDF
Name:
Trismus-pseudocamptodactyly syndrome
Description:
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.
ORPHAcode:
3377
Synonyms:
Distal arthrogryposis type 7
Dutch-Kentucky syndrome
Hecht syndrome
Hecht-Beals syndrome
XREF(s):
Orphanet
OMIM
ICD-10
Analyte(s):
MYH8
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14