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- Q1286320 subject Q11052013.
- Q1286320 abstract "Schwannomatosis is one form of a genetic disorder called neurofibromatosis (NF) that has only recently been recognized. Originally described in Japanese patients, it consists of multiple cutaneous schwannomas, central nervous system tumors, and other neurological complications, excluding hallmark signs of NF. It is a rare disorder, affecting only around 1 in 40,000 individuals.Schwannomas are mostly benign tumors that commonly occur in individuals with NF2 and schwannomatosis (sometimes called neurofibromatosis type III). Schwann cells are glial cells that myelinate the axons of nerve cells. Myelin is a lipid covering that speeds the conduction of action potentials. When Schwann cells proliferate out of control in an encapsulation it is called a schwannoma. Although schwannomas are benign they become detrimental when the growing tumor compresses the nerve. Schwannomas on sensory nerve axons cause chronic severe pain. Treatment options for schwannomas are to surgically remove them, have radiation, cyberknife or Intracapsular Enucleation. Previous designations for schwannomas include neurinoma and neurilemmoma.".
- Q1286320 omim "162091".
- Q1286320 wikiPageWikiLink Q1074.
- Q1286320 wikiPageWikiLink Q11052013.
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- Q1286320 wikiPageWikiLink Q5552256.
- Q1286320 wikiPageWikiLink Q7616509.
- Q1286320 wikiPageWikiLink Q847605.
- Q1286320 name "Schwannomatosis".
- Q1286320 omim "162091".
- Q1286320 type Disease.
- Q1286320 type Thing.
- Q1286320 type Q12136.
- Q1286320 comment "Schwannomatosis is one form of a genetic disorder called neurofibromatosis (NF) that has only recently been recognized. Originally described in Japanese patients, it consists of multiple cutaneous schwannomas, central nervous system tumors, and other neurological complications, excluding hallmark signs of NF.".
- Q1286320 label "Schwannomatosis".
- Q1286320 name "Schwannomatosis".