KEGG   DISEASE: 発作性激痛症
エントリ  
H00772                                                             
名称    
発作性激痛症
概要    
Paroxysmal extreme pain disorder (PEPD) is an autosomal dominant pain disorder resulting from a set of gain-of-function mutations in SCN9A, the gene encoding Nav1.7, that impair inactivation of Nav1.7. Severe pain in PEPD patients along with flushing is induced by bowel movement or probing of the perianal areas, and is sometimes accompanied by tonic nonepileptic seizures and cardiac deficits. The pain attacks are most severe in the lower part of the body and are often triggered by temperature changes (such as cold winds), eating, and/or emotional upsets (such as crying).
カテゴリ  
神経系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  神経系のその他の疾患
   8E43  疼痛障害
    H00772  発作性激痛症
病因遺伝子 
SCN9A [HSA:6335] [KO:K04841]
リンク   
ICD-11: 8E43.Y
MeSH: C563475
OMIM: 167400
文献    
  著者
Catterall WA, Dib-Hajj S, Meisler MH, Pietrobon D
  タイトル
Inherited neuronal ion channelopathies: new windows on complex neurological diseases.
  雑誌
J Neurosci 28:11768-77 (2008)
DOI:10.1523/JNEUROSCI.3901-08.2008
文献    
  著者
Dib-Hajj SD, Yang Y, Waxman SG
  タイトル
Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes.
  雑誌
Adv Genet 63:85-110 (2008)
DOI:10.1016/S0065-2660(08)01004-3
文献    
  著者
Fischer TZ, Waxman SG
  タイトル
Familial pain syndromes from mutations of the NaV1.7 sodium channel.
  雑誌
Ann N Y Acad Sci 1184:196-207 (2010)
DOI:10.1111/j.1749-6632.2009.05110.x
LinkDB    

» English version

DBGET integrated database retrieval system