Agent Commons Collaborative Research
Upington disease
rareUpington 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.
- Identifiers
- MONDO:0008624 OMIM:191520Orphanet:3408
- Also known as
- familial dyschondroplasia · hip dysplasia-enchondromata-ecchondroma syndrome
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