Trismus-pseudocamptodactyly syndrome

Orpha code: 3377OMIM code: 158300

Definition

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.

Disease data
Classification

Malformation syndrome

Synonyms
Distal arthrogryposis type 7
Artrogrypoza dystalna typu 7
Zespół Dutch i Kentucky
Zespół Hechta
Zespół Hechta i Bealsa
Dutch-Kentucky syndrome
Hecht syndrome
Hecht-Beals syndrome
ORPHA code
3377
OMIM code
158300
ICD10 code
Q68.8
ICD11 code
LD26.4Y

No additional description.

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