Atelosteogenesis type II

A rare, lethal perinatal bone dysplasia characterized by limb shortening, normal sized skull with cleft palate, hitchhiker thumbs, distinctive facial dysmorphism and radiographic skeletal features, caused by mutations in the diastrophic dysplasia sulfate transporter gene.

Upper limb undergrowth

Arm shortening because of underdevelopment of one or more bones of the upper extremity.


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PMID (PMCID)