KEGG   DISEASE: Paroxysmal extreme pain disorder
Entry
H00772                      Disease                                
Name
Paroxysmal extreme pain disorder
Description
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).
Category
Nervous system disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 08 Diseases of the nervous system
  Other disorders of the nervous system
   8E43  Pain disorders
    H00772  Paroxysmal extreme pain disorder
Gene
SCN9A [HSA:6335] [KO:K04841]
Other DBs
ICD-11: 8E43.Y
MeSH: C563475
OMIM: 167400
Reference
  Authors
Catterall WA, Dib-Hajj S, Meisler MH, Pietrobon D
  Title
Inherited neuronal ion channelopathies: new windows on complex neurological diseases.
  Journal
J Neurosci 28:11768-77 (2008)
DOI:10.1523/JNEUROSCI.3901-08.2008
Reference
  Authors
Dib-Hajj SD, Yang Y, Waxman SG
  Title
Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes.
  Journal
Adv Genet 63:85-110 (2008)
DOI:10.1016/S0065-2660(08)01004-3
Reference
  Authors
Fischer TZ, Waxman SG
  Title
Familial pain syndromes from mutations of the NaV1.7 sodium channel.
  Journal
Ann N Y Acad Sci 1184:196-207 (2010)
DOI:10.1111/j.1749-6632.2009.05110.x
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