KEGG   DISEASE: 妊娠性肝内胆汁うっ滞
エントリ  
H02193                                                             
名称    
妊娠性肝内胆汁うっ滞
概要    
Intrahepatic cholestasis of pregnancy (ICP), also called obstetric cholestasis, is the most common pregnancy-specific liver disease. Classic symptoms include generalized pruritus that commonly includes the palms and soles, and biochemical evidence of elevated bile acids, with or without elevated liver function tests (LFTs). The etiology of ICP is influenced by a combination of genetic, endocrine, and environmental factors. Risk factors for ICP include multiple pregnancy, in vitro fertilization, advanced maternal age, history of prior affected pregnancy, positive family history, and hepatitis C infection.
カテゴリ  
消化器系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 18 妊娠, 分娩, 産褥
  主として妊娠に関連する明示された母体疾患
   JA65  主として妊娠に関連するその他の病態の母体ケア
    H02193  妊娠性肝内胆汁うっ滞
パスウェイ 
hsa04976  Bile secretion
病因遺伝子 
(ICP1) ATP8B1 [HSA:5205] [KO:K01530]
(ICP3) ABCB4 [HSA:5244] [KO:K05659]
リンク   
ICD-11: JA65.0
MeSH: D002780
OMIM: 147480 614972
文献    
  著者
Wood AM, Livingston EG, Hughes BL, Kuller JA
  タイトル
Intrahepatic Cholestasis of Pregnancy: A Review of Diagnosis and Management.
  雑誌
Obstet Gynecol Surv 73:103-109 (2018)
DOI:10.1097/OGX.0000000000000524
文献    
  著者
McIlvride S, Dixon PH, Williamson C
  タイトル
Bile acids and gestation.
  雑誌
Mol Aspects Med 56:90-100 (2017)
DOI:10.1016/j.mam.2017.05.003
文献    
  著者
Ovadia C, Williamson C
  タイトル
Intrahepatic cholestasis of pregnancy: Recent advances.
  雑誌
Clin Dermatol 34:327-34 (2016)
DOI:10.1016/j.clindermatol.2016.02.004
文献    
  著者
Mullenbach R, Bennett A, Tetlow N, Patel N, Hamilton G, Cheng F, Chambers J, Howard R, Taylor-Robinson SD, Williamson C
  タイトル
ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.
  雑誌
Gut 54:829-34 (2005)
DOI:10.1136/gut.2004.058115
文献    
PMID:9419367
  著者
de Vree JM, Jacquemin E, Sturm E, Cresteil D, Bosma PJ, Aten J, Deleuze JF, Desrochers M, Burdelski M, Bernard O, Oude Elferink RP, Hadchouel M
  タイトル
Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis.
  雑誌
Proc Natl Acad Sci U S A 95:282-7 (1998)
DOI:10.1073/pnas.95.1.282
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