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Coexistence of Gilbert syndrome with hereditary haemolytic anaemias.

Rawa, Katarzyna and Adamowicz-Salach, Anna and Matysiak, Michal and Trzemecka, Anna and Burzynska, Beata (2012) Coexistence of Gilbert syndrome with hereditary haemolytic anaemias. Journal of clinical pathology, 65 (7). pp. 663-5. ISSN 1472-4146

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Abstract

Genotyping of the UGT1A1 gene showed distinct distribution of the common A(TA)(n)TAA polymorphism relative to other European populations. Because of a greater risk of hyperbilirubinaemia due to hereditary haemolytic anaemia, the diagnosis of Gilbert syndrome in this group of patients is very important.

Item Type:Article
Subjects:Q Science > QH Natural history > QH426 Genetics
R Medicine > R Medicine (General)
Divisions:Department of Genetics
ID Code:472
Deposited By: Dr Beata Burzynska
Deposited On:11 Mar 2013 08:24
Last Modified:11 Mar 2013 08:24

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