维基百科中的医学内容
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吉尔波特症候群(英语:Gilbert's syndrome,简称GS)为一种常见的遗传性肝脏疾病,盛行率约3-12%[1][2][3][4][5]。
Quick Facts 吉尔波特症候群, 同义词 ...
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患者体内的非共轭性胆红素会显著提升,但没有明显并发症,患者可能会在运动后产生轻微黄疸。
造成此疾病的原因为患者的葡萄糖醛酸苷转移酶功能不佳[6][7],使非共轭胆红素无法转化为较为水溶的共轭胆红素。
Dugdale, David C. Gilbert's disease. MedlinePlus. U.S. National Library of Medicine. 2013-05-13 [10 February 2014]. (原始内容存档于2016-07-05).
Bosma, PJ; Chowdhury, JR; Bakker, C; Gantla, S; de Boer, A; Oostra, BA; Lindhout, D; Tytgat, GN; Jansen, PL; Oude Elferink, RP. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.. The New England Journal of Medicine. 2 November 1995, 333 (18): 1171–5. PMID 7565971. doi:10.1056/nejm199511023331802.
Koiwai, O; Nishizawa, M; Hasada, K; Aono, S; Adachi, Y; Mamiya, N; Sato, H. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.. Human Molecular Genetics. July 1995, 4 (7): 1183–6. PMID 8528206. doi:10.1093/hmg/4.7.1183.
Foulk, WT; Butt, HR; Owen, CA Jr; Whitcomb, FF Jr; Mason, HL. Constitutional hepatic dysfunction (Gilbert's disease): its natural history and related syndromes. Medicine (Baltimore). 1959, 38 (1): 25–46. PMID 13632313.
Wire preaches delights of three cliffs. South Wales Evening Post. 2007-04-27: 3.