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Hapnes Boman Skeie syndrome



Hapnes Boman Skeie syndrome is a rare genetic disorder in which subcutaneous angiolipomas form around the wrists, knees, and ankles. [2] The syndrome was first described by Sveln Hapnes et al. in 1980. [2]

Hapnes Boman Skeie syndrome
Other namesExtensor tendons of finger anomalies[1]
This condition is inherited in an autosomal dominant manner

Hapnes Boman Skeie syndrome is also known as "anomalous insertion of extensor tendons of fingers".[3] This name derives from the condition that the tendons of the fingers are attached in such a way that the fingers cannot open or close normally. Though the tumors extend deeply into the muscle tissue, joints, and tendons, the tumors did not invade these structures.[2]


References

  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Extensor tendons of finger anomalies" . www.orpha.net. Retrieved 24 October 2019.
  2. ^ a b c Hapnes, Sveln A.; Boman, Helge; Seele, Sverre O. (March 1980). "Familial angiolipomatosis". Clinical Genetics. 17 (3): 202–208. doi:10.1111/j.1399-0004.1980.tb00133.x . PMID 7363507 . S2CID 12632218 .
  3. ^ "Tendons, extensor, of fingers, anomalous insertion of" . Genetic & Rare Diseases Information Center. Retrieved 2012-10-31.

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Information as of: 20.08.2021 03:10:34 CEST

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