Hardcastle_syndrome

Hardcastle syndrome

Hardcastle syndrome

Medical condition

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]

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References

  1. [1]
    McKusick, Victor A.; Kniffin, Cassandra L. (30 June 2015). "OMIM Entry - # 112250 - Diaphyseal medullary stenosis with malignant fibrous histiocytoma; DMSMFH". OMIM. Retrieved 2019-06-05.
  2. [2]
    Bissonnette, Bruno; Luginbuehl, Igor; Marciniak, Bruno; Dalens, Bernard J. (2006), "Hardcastle Syndrome", Syndromes: Rapid Recognition and Perioperative Implications, The McGraw-Hill Companies, retrieved 2019-06-05
  3. [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. S2CID 9795563.
  4. [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. [5]
    "Hardcastle syndrome". TheFreeDictionary.com. Retrieved 2019-06-05.











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