KEGG   DISEASE: Chronic idiopathic intestinal pseudo-obstruction
Entry
H01276                      Disease                                
Name
Chronic idiopathic intestinal pseudo-obstruction;
CIIP
Description
Chronic idiopathic intestinal pseudo-obstruction (CIIP) is a rare, often fatal syndrome, caused by a heterogeneous group of enteric neuromuscular diseases that result in a severe abnormality of gastrointestinal motility. The typical clinical manifestation is characterized by recurrent episodes of abdominal pain, abdominal distension, and inability to defecate. CIIP is one of the most important causes of chronic intestinal failure both in pediatric and adult cases, since affected individuals are often unable to maintain normal body weight and/or normal oral nutrition. CIIP is generally sporadic, but familial forms have also been described. It has been reported that flamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction.
Category
Digestive system disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 13 Diseases of the digestive system
  Diseases of small intestine
   DA90  Nonstructural developmental anomalies of small intestine
    H01276  Chronic idiopathic intestinal pseudo-obstruction
Pathway
hsa04010  MAPK signaling pathway
hsa04510  Focal adhesion
Gene
FLNA [HSA:2316] [KO:K04437]
Other DBs
ICD-11: DA90.2
MeSH: D007418
OMIM: 300048
Reference
  Authors
Antonucci A, Fronzoni L, Cogliandro L, Cogliandro RF, Caputo C, De Giorgio R, Pallotti F, Barbara G, Corinaldesi R, Stanghellini V
  Title
Chronic intestinal pseudo-obstruction.
  Journal
World J Gastroenterol 14:2953-61 (2008)
DOI:10.3748/wjg.14.2953
Reference
  Authors
Gargiulo A, Auricchio R, Barone MV, Cotugno G, Reardon W, Milla PJ, Ballabio A, Ciccodicola A, Auricchio A
  Title
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement.
  Journal
Am J Hum Genet 80:751-8 (2007)
DOI:10.1086/513321
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