Literature DB >> 3608845

[Prevalence of Gilbert's syndrome in Germany].

A Sieg, L Arab, G Schlierf, A Stiehl, B Kommerell.   

Abstract

The prevalence of Gilbert's syndrome was studied in a randomized group of 1530 persons (785 men and 745 women, aged 20-40 years) living in the Heidelberg region of the Federal Republic of Germany. It was found to be present in 12.4% of men and 4.8% of women, i.e. a total of 8.6% for the entire group. In women the serum bilirubin level (mean 12.0 +/- 5.1 mumol/l) was significantly lower than in men (mean of 13.7 +/- 6.8 mumol/l; P less than 0.001). Analysing the frequency distribution of serum bilirubin revealed that patients with this syndrome do not constitute a population of its own, but rather form the upper end of the normative bilirubin distribution curve.

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Year:  1987        PMID: 3608845     DOI: 10.1055/s-2008-1068222

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN: 0012-0472            Impact factor:   0.628


  17 in total

1.  Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene.

Authors:  Shabana Farheen; Sanghamitra Sengupta; Amal Santra; Suparna Pal; Gopal Krishna Dhali; Meenakshi Chakravorty; Partha P Majumder; Abhijit Chowdhury
Journal:  World J Gastroenterol       Date:  2006-04-14       Impact factor: 5.742

2.  Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.

Authors:  Yoshihiro Maruo; Yoriko Morioka; Hiroshi Fujito; Sayuri Nakahara; Takahide Yanagi; Katsuyuki Matsui; Asami Mori; Hiroshi Sato; Robert H Tukey; Yoshihiro Takeuchi
Journal:  J Pediatr       Date:  2014-03-17       Impact factor: 4.406

3.  Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.

Authors:  Akitaka Nomura; Yoshihiro Maruo; Takashi Taga; Yoshihiro Takeuchi
Journal:  Pediatr Res       Date:  2016-04-08       Impact factor: 3.756

4.  Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

Authors:  Jae Hee Lee; Kyung Rye Moon
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2014-12-31

5.  Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome.

Authors:  Katsuyuki Matsui; Yoshihiro Maruo; Hiroshi Sato; Yoshihiro Takeuchi
Journal:  BMC Gastroenterol       Date:  2010-06-08       Impact factor: 3.067

6.  Pharmacokinetics of morphine are not altered in subjects with Gilbert's syndrome.

Authors:  Carsten Skarke; Helmut Schmidt; Gerd Geisslinger; Jutta Darimont; Jörn Lötsch
Journal:  Br J Clin Pharmacol       Date:  2003-08       Impact factor: 4.335

7.  Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?

Authors:  E Beutler; T Gelbart; A Demina
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-07       Impact factor: 11.205

8.  Crigler-Najjar syndrome type II. New observation of possible autosomal recessive inheritance.

Authors:  S Güldütuna; U Langenbeck; K W Bock; A Sieg; U Leuschner
Journal:  Dig Dis Sci       Date:  1995-01       Impact factor: 3.199

9.  Multiple variants in UGT1A1 gene are factors to develop indirect hyper-bilirubinemia.

Authors:  Rei-Ting Hu; Nai-Yuan Wang; May-Jen Huang; Ching-Shan Huang; Ding-Shinn Chen; Sien-Sing Yang
Journal:  Hepatobiliary Surg Nutr       Date:  2014-08       Impact factor: 7.293

10.  Gilbert syndrome in Iran, Fars Province.

Authors:  Fariba Hemmati; Forugh Saki; Nasrin Saki; Mahmood Haghighat
Journal:  Ann Saudi Med       Date:  2010 Jan-Feb       Impact factor: 1.526

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