Medicine:Hardcastle syndrome

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Hardcastle syndrome
Other namesBone dysplasia-medullary fibrosarcoma syndrome, diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Autosomal dominant - en.svg
Hardcastle syndrome is inherited in an autosomal dominant pattern.[1]

Hardcastle syndrome is a rare genetic disorder on chromosome 9 at 9p22-p21.[2] It affects the long bones.[3][4] There is a high risk for histiocytoma.[5]

References

  1. McKusick, Victor A.; Kniffin, Cassandra L. (30 June 2015). "OMIM Entry - # 112250 - Diaphyseal medullary stenosis with malignant fibrous histiocytoma; DMSMFH". https://omim.org/entry/112250. 
  2. Bissonnette, Bruno; Luginbuehl, Igor; Marciniak, Bruno; Dalens, Bernard J. (2006), "Hardcastle Syndrome", Syndromes: Rapid Recognition and Perioperative Implications (The McGraw-Hill Companies), http://accessanesthesiology.mhmedical.com/content.aspx?aid=58079211, retrieved 2019-06-05 
  3. Norton, K. I.; Wagreich, J. M.; Granowetter, L.; Martignetti, J. A. (September 1996). "Diaphyseal medullary stenosis (sclerosis) with bone malignancy (malignant fibrous histiocytoma): Hardcastle syndrome". Pediatric Radiology 26 (9): 675–677. doi:10.1007/BF01356833. ISSN 0301-0449. PMID 8781110. 
  4. Jamil, Wiqqas; Allami, Mohammad K.; Mbakada, Nikita; Kluge, Wolfram (December 2009). "Total knee arthroplasty in a patient with Hardcastle syndrome". Orthopedics 32 (12): 916. doi:10.3928/01477447-20091020-20. ISSN 1938-2367. PMID 19968223. 
  5. "Hardcastle syndrome". https://medical-dictionary.thefreedictionary.com/Hardcastle+syndrome. 











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Classification