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Xu, C. Gilbert Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4004 (accessed on 27 September 2026).
Xu C. Gilbert Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4004. Accessed September 27, 2026.
Xu, Camila. "Gilbert Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4004 (accessed September 27, 2026).
Xu, C. (2020, December 23). Gilbert Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4004
Xu, Camila. "Gilbert Syndrome." Encyclopedia. Web. 23 December, 2020.
Gilbert Syndrome
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/gilbert-syndrome

Gilbert syndrome is a relatively mild condition characterized by periods of elevated levels of a toxic substance called bilirubin in the blood (hyperbilirubinemia).

genetic conditions

References

  1. Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP, et al. The genetic basis of the reducedexpression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. NEngl J Med. 1995 Nov 2;333(18):1171-5.
  2. Bosma PJ. Inherited disorders of bilirubin metabolism. J Hepatol. 2003Jan;38(1):107-17. Review.
  3. Fretzayas A, Moustaki M, Liapi O, Karpathios T. Gilbert syndrome. Eur JPediatr. 2012 Jan;171(1):11-5. doi: 10.1007/s00431-011-1641-0.Review.
  4. Udomuksorn W, Elliot DJ, Lewis BC, Mackenzie PI, Yoovathaworn K, Miners JO.Influence of mutations associated with Gilbert and Crigler-Najjar type IIsyndromes on the glucuronidation kinetics of bilirubin and otherUDP-glucuronosyltransferase 1A substrates. Pharmacogenet Genomics. 2007Dec;17(12):1017-29.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 886
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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