CLOVES syndrome

CLOVES syndrome is an extremely rare overgrowth syndrome, with complex vascular anomalies. CLOVES syndrome affects people with various symptoms, ranging from mild soft-tissue tumors to vascular malformations encompassing the spine or internal organs. CLOVES syndrome is closely linked to other overgrowth disorders like proteus syndrome, Klippel–Trénaunay syndrome, Sturge–Weber syndrome, and hemihypertrophy, to name a few.

'CLOVES' is an acronym for:[1][2]

It is believed that the first description of a case of CLOVES syndrome was written by Hermann Friedberg, a German physician, in 1867.[3][4]

References

  1. "CLOVES Syndrome". clovessyndrome.org.
  2. Boston Childrens Hospital 2013. "CLOVES Syndrome - Boston Children's Hospital". childrenshospital.org.
  3. "CLOVES Syndrome". National Organization for Rare Diseases. Retrieved 24 March 2015.
  4. Alomari, AI; Thiex, R; Mulliken, JB (October 2010). "Hermann Friedberg's case report: an early description of CLOVES syndrome". Clinical Genetics 78 (4): 342–347. doi:10.1111/j.1399-0004.2010.01479.x.

Externalk links

This article is issued from Wikipedia - version of the Thursday, May 05, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.