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Osebold-Remondini syndrome
rareA 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.
- Identifiers
- MONDO:0007219 OMIM:112910Orphanet:93382
- 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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