Results 11 to 20 of about 1,143,701 (190)
Diagnosis of Gilbert's Syndrome in Checkup Tests: Case Report [PDF]
Archives of Advances in Biosciences, 2023 Introduction: Gilbert's syndrome (GS) is an autosomal recessive condition characterized by a relative lack of glucuronyl transferase, inadequate hepatocyte absorption of unconjugated bilirubin, and recurrent bouts of jaundice.
Mohadeseh Rostamipoor +2 more
doaj +2 more sources
Age and gender distribution among the patients with Gilbert’s syndrome
Фундаментальная и клиническая медицина, 2021 Aim. To analyze age and gender distribution in patients with Gilbert's syndrome.Materials and Methods. We consecutively recruited 115 patients with Gilbert's syndrome. All patients underwent genotyping of the rs8175347 polymorphism within the UGT1A1 gene
A. N. Volkov, E. V. Tsurkan
doaj +2 more sources
Combination of Gilbert's syndrome and gastrointestinal diseases [PDF]
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2014 The aim of review. To detect relation between Gilbert's syndrome (GS) and other diseases of a gastrointestinal tract (GIT).Key points. Gilbert's syndrome - hereditary, unconjugated jaundice related to decrease of activity of uridinediphosphate ...
G. M. Dubrovina +2 more
doaj +1 more source
Allogeneic hematopoietic stem cell transplantation for acute leukemia with Gilbert's syndrome [PDF]
Journal of Hematology & Oncology, 2011 Acute leukemia with coexisting Gilbert's syndrome treated by allogeneic hematopoietic stem cell transplantation (allo-HSCT) is rarely reported. Here we described a case whose transaminase levels were almost normal, although transient hyperbilirubinemia ...
Sun Jing +7 more
doaj +2 more sources
The Mutation Hotspots at UGT1A Locus May Be Associated with Gilbert's Syndrome Affecting the Taiwanese Population. [PDF]
Int J Mol Sci, 2022 [[abstract]]Gilbert's syndrome is mainly diagnosed through genetic analysis and is primarily detected through a mutation in the promoter region of the UGT1A1 gene. However, most of the research has been conducted on Caucasian populations.
Hsu PW +8 more
europepmc +2 more sources
(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome
Haematologica, 1999 BACKGROUND AND OBJECTIVE: Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinemia, is caused by a reduction in the activity of hepatic bilirubin UDP-glucuronosyltransferase (UGT1A1).
A Iolascon +5 more
doaj +3 more sources
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates
Haematologica, 1999 BACKGROUND AND OBJECTIVE: The pathogenesis of the hyperbilirubinemia present in approximately 30% of neonates affected by glucose-6-phosphate dehydrogenase deficiency is an unsolved problem.
A Iolascon +5 more
doaj +1 more source
Food Faddism Complicating Jaundice in Gilbert’s Syndrome Patients- A Prospective Cohort Study [PDF]
Journal of Clinical and Diagnostic Research, 2022 Introduction: Food faddism is a term that refers to a particular food or food group that is overemphasised in the regular diet or omitted to cure a specific condition.
Pentakota Kiranmayi +2 more
doaj +1 more source
Turkish Journal of Internal Medicine, 2022 Gilbert’s syndrome is a genetic disorder characterised by non-hemolytic unconjugated hyperbilirubinemia. It is caused by mutations in the UGT1A1 gene which codes for the enzyme uridine diphosphate glucoronosyl transferase-1, which conjugates bilirubin ...
Devyani Thakur, Yogita Sharma
doaj +1 more source
Hepatology, EarlyView., 2022 A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan +19 more
wiley +1 more source