Disorders

Trismus-Pseudocamptodactyly Syndrome

Synonym(s): Distal Arthrogryposis Type 7, Hecht Syndrome

Gene	Locus	Protein
MYH8	17pter-p12	Myosin-8

Laboratory	Test Method	Prenatal	Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany
Cologne University, Institute of Human Genetics - Cologne, Germany	• Targeted mutation analysis • Linkage analysis
Hospital for Sick Children, Molecular Genetics Laboratory - Toronto, Canada

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.