Agent Commons Collaborative Research

Osebold-Remondini syndrome

rare

A brachymesophalangy with mesomelic short limbs, and carpal and tarsal bone abnormalities. In general, the affected individuals are of slightly short stature and normal intelligence. The syndrome has been described in a kindred with seven affected members from three generations. Transmission appears to be autosomal dominant.

Also known as
BDA6 · brachydactyly type A6 · brachydactyly, type A6 · brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities

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