Rosatelli M C, Meloni A, Faa V, Saba L, Crisponi G, Clemente M G, Meloni G, Piga M T, Cao A
Instituto di Clinica e Biologia dell'Età Evolutiva, Università degli Studi di Cagliari, Sardinia, Italy.
J Med Genet. 1997 Feb;34(2):122-5. doi: 10.1136/jmg.34.2.122.
This study reports the molecular characterisation of the bilirubin UDP-glucuronosyl-transferase gene (UGT1) in a group of patients of Sardinian descent with Crigler-Najjar syndrome type I and their relatives. Sequence analysis of both UGT1A exon 1 and common exons 2-5 was performed in all patients, leading to the detection of AF170 and a novel mutation (470insT), both residing in UGT1A exon 1. All but two heterozygotes for the AF170 mutation showed normal serum bilirubin levels. These two subjects were also heterozygous for the sequence variation A(TA)7TAA in the promoter region of the UGT1A gene.
本研究报告了一组撒丁岛血统、患有I型克里格勒-纳贾尔综合征的患者及其亲属中胆红素UDP-葡萄糖醛酸基转移酶基因(UGT1)的分子特征。对所有患者的UGT1A外显子1以及常见外显子2至5进行了序列分析,结果在UGT1A外显子1中检测到AF170和一种新的突变(470insT)。除两名AF170突变杂合子外,其他所有患者血清胆红素水平均正常。这两名患者在UGT1A基因启动子区域的序列变异A(TA)7TAA中也是杂合子。