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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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