Sandrow syndrome of mirror hands and feet and facial abnormalities
Related Experiment Videos
N Kogekar1, A S Teebi, J Vockley
1Department of Genetics, Yale University School of Medicine, New Haven, Connecticut.
American Journal of Medical Genetics
|April 15, 1993
Abstract:
In 1970, Sandrow et al. (J Bone Joint Surg 52-A:363-370) described a syndrome of ulnar and fibular dimelia with facial abnormalities present in 2 generations in a family. We describe a new patient with similar manifestations, establishing this constellation of anomalies as a distinct syndrome.