KEGG   DISEASE: 先天性無痛覚
エントリ  
H00774                                                             
名称    
先天性無痛覚
  下位グループ
Marsili 症候群
概要    
Congenital insensitivity to pain (CIP) is condition affecting pain sensation and olfaction. A loss-of-function of the SCN9A, the gene encoding Nav1.7, can produce CIP. Patients with Nav1.7-related CIP present with a history of not ever experiencing any pain even after burns, bone fractures, lip- and tongue-biting, and they do not experience visceral pain. Additionally, patients with Nav1.7-related CIP do not show apparent sympathetic dysfunction and have a normal axon reflex response to histamine. Homozygous and compound null mutations in SCN9A are predicted to truncate the channel protein, resulting in loss-of-function mutations in Nav1.7 and the complete loss of Nav1.7 current in all of the neurons in which this channel is expressed. Marsili syndrome(MARSIS) is an autosomal dominant congenital insensitivity to pain, caused by mutations in ZFHX2 gene.
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
  神経根, 神経叢または末梢神経の疾患
   遺伝性ニューロパチー
    8C21  遺伝性感覚または自律神経ニューロパチー
     H00774  先天性無痛覚
病因遺伝子 
(CIP) SCN9A [HSA:6335] [KO:K04841]
(MARSIS) ZFHX2 [HSA:85446] [KO:K09379]
リンク   
ICD-11: 8C21.3
MeSH: D000699
OMIM: 243000 147430
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
文献    
PMID:29253101 (MARSIS)
  著者
Habib AM, Matsuyama A, Okorokov AL, Santana-Varela S, Bras JT, Aloisi AM, Emery EC, Bogdanov YD, Follenfant M, Gossage SJ, Gras M, Humphrey J, Kolesnikov A, Le Cann K, Li S, Minett MS, Pereira V, Ponsolles C, Sikandar S, Torres JM, Yamaoka K, Zhao J, Komine Y, Yamamori T, Maniatis N, Panov KI, Houlden H, Ramirez JD, Bennett DLH, Marsili L, Bachiocco V, Wood JN, Cox JJ
  タイトル
A novel human pain insensitivity disorder caused by a point mutation in ZFHX2.
  雑誌
Brain 141:365-376 (2018)
DOI:10.1093/brain/awx326
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