Osebold-Remondini syndrome
MONDO:0007219A 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, Osebold-Remondini syndrome, brachydactyly type A6, brachydactyly, type A6, brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities, Brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities, OSEBOLD-Remondini syndrome
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