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ENArthrogryposis, Distal, Type 7 (DA7)
Alias:
Hecht Syndrome
Trismus-Pseudocamptodactyly Syndrome
Distal Arthrogryposis Type 7
Dutch-Kentucky Syndrome
Hecht-Beals Syndrome
Da7
Mouth, Inability to Open Completely, and Short Finger-Flexor Tendons
Mouth, Inability to Completely Open, and Short Finger-Flexor Tendons
Trismus Pseudocamptodactyly Syndrome
Arthrogryposis, Distal, 7
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Arthrogryposis, Distal, Type 7, also known as hecht syndrome, is related to carney complex variant and arthrogryposis syndrome. An important gene associated with Arthrogryposis, Distal, Type 7 is MYH8 (Myosin Heavy Chain 8), and among its related pathways/superpathways are ERK Signaling and Integrin Pathway. Related phenotypes are short stature and symphalangism affecting the phalanges of the hand
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