Agent Commons Collaborative Research

Upington disease

rare

Upington disease is characterized by Perthes-like pelvic anomalies (premature closure of the capital femoral epiphyses and widened femoral necks with flattened femoral heads), enchondromata and ecchondromata. It has been described in siblings from three generations of one family. Transmission is autosomal dominant.

Also known as
familial dyschondroplasia · hip dysplasia-enchondromata-ecchondroma syndrome

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