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Gilbert syndrome (GS) is an autosomal recessive inherited disorder of bilirubin glucuronidation which has not been investigated in Egypt. This longitudinal study investigated the frequency, clinical course, genetic profile and health related quality of life in Egyptian adults.
- PubMed
Background and aims: Gilbert's syndrome is a common familial...
- PubMed
Background and aims: Gilbert's syndrome is a common familial hyperbilirubinemia that may reduce the risk of various age-related diseases because of the antioxidant properties of bilirubin. We conducted a large cohort study using The Health Improvement Network primary care database and compared all-cause mortality rates in those with and without ...
Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine laboratory check-ups or after an intercurrent illness. The diagnosis is typically made per exclusionem, i.e. by excluding other causes of hyperbilirubinaemia.
5 Οκτ 2024 · This activity for healthcare professionals reviews the etiology, epidemiology, pathophysiology, clinical presentation, recommended evaluation, and management of Gilbert syndrome and highlights the role of the interprofessional team in improving the quality of life and outcomes for patients with this genetic disorder.
6 Σεπ 2022 · Gilbert syndrome (GS) is a genetic syndrome of mild unconjugated hyperbilirubinaemia, by definition <102 micromol/L (<6 mg/dL) (rarely exceeding 68.4 micromol/L [4 mg/dL]). The liver function is otherwise normal. Common syndrome affecting approximately 6% of the general population.
Individuals with Gilbert's syndrome have an increased incidence of gallstones, but it is well known that carriers are not at significant risk for progressive liver disease; the condition does...
13 Δεκ 2018 · Goals: Investigation of the frequency clinical spectrum, genetic profile and health related quality of life (HRQOL) in Egyptian with Gilbert syndrome (GS).
