C122660Level 6
Hardcastle's Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** A rare, autosomal dominant inherited dysplasia of the long bones, characterized by symmetrical diaphyseal medullary stenosis, bone infarctions, pathologic fractures, and a high risk of development of malignant fibrous histiocytoma.
**Synonyms:** - DMS-MFH - Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma
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