Diagnosis and treatment of a 16-year-old Chinese patient with concurrent hereditary hemochromatosis and Gilbert's syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s40001-014-0051-y.pdf
Reference18 articles.
1. Andrews NC: Molecular control of iron metabolism. Best Pract Res Clin Haematol 2005, 18: 159–169. 10.1016/j.beha.2004.10.004
2. Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury JR, Chowdhury NR: Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. Hum Mutat 2000, 16: 297–306. 10.1002/1098-1004(200010)16:4<297::AID-HUMU2>3.0.CO;2-Z
3. Lee JY, Yoo KH, Hahn SH: HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasian is extremely rare in Korean population. J Korean Medical Sci 2000, 15: 179–182. 10.3346/jkms.2000.15.2.179
4. Hanson EH, Imperatore G, Burke W: HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology 2001, 154: 193–206.
5. Claridge LC, Armstrong MJ, Booth C, Gill PS: Gilbert’s syndrome. BMJ 2011, 342: d2293. 10.1136/bmj.d2293
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