Literature DB >> 14555319

Gilbert's syndrome as a predisposing factor for idiopathic cholelithiasis in children.

Sofia Kitsiou-Tzeli, Emmanuel Kanavakis, Maria Tzetis, Emmanuel Kavazarakis, Angeliki Galla, Aspasia Tsezou.   

Abstract

The frequency of the (TA)7/(TA)7 promoter genotype of UDP-glucuronosyltransferase gene (UGT1A1) was significantly higher (p<0.05) in a group of 30 children with cholelithiasis than in a control group of 40 healthy children, indicating that this genotype might be an underlying factor for gallstone initiation in otherwise healthy children.

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Year:  2003        PMID： 14555319

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


  4 in total

Review 1.  Gilbert syndrome.

Authors:  Andrew Fretzayas; Maria Moustaki; Olga Liapi; Themistocles Karpathios
Journal:  Eur J Pediatr       Date:  2011-12-09       Impact factor: 3.183

2.  Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.

Authors:  Shigeo Iijima; Takehiko Ohzeki; Yoshihiro Maruo
Journal:  Yonsei Med J       Date:  2011-03       Impact factor: 2.759

3.  Gilbert's Syndrome in Children with Unconjugated Hyperbilirubinemia - An Analysis of 170 Cases.

Authors:  Vikrant Sood; Bikrant Bihari Lal; Shvetank Sharma; Rajeev Khanna; Manish K Siloliya; Seema Alam
Journal:  Indian J Pediatr       Date:  2020-03-27       Impact factor: 1.967

4.  Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome.

Authors:  Ling-Ling Kang; Yong-Jian Ma; Hou-De Zhang
Journal:  Medicine (Baltimore)       Date:  2020-02       Impact factor: 1.817
  4 in total

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