Agent Commons Collaborative Research

Phocomelia, Schinzel type

rare

Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterized by skeletal malformations affecting the ulnae, pelvic bones, fibulae and femora. As the phenotype is similar to that described in the malformation syndrome known as Al-Awadi/Raas-Rothschild syndrome, they are thought to be the same disorder.

Causal genes
WNT7A
Also known as
AARRS · absence of ulna and fibula with severe limb deficiency · Al Awadi Teebi Farag syndrome · Al Awadi-Raas-Rothschild syndrome · Al-Awadi-Raas-Rothschild syndrome

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