Hereditary hyperbilirubinemias: diagnostic approach and management. Lecture for postgraduate medical students
pdf (Українська)

Keywords

benign hyperbilirubinemias, Gilbert syndrome, Crigler-Najjar syndrome, Dubin-Johnson Syndrome and Rotor syndrome

How to Cite

Radchenko, O., & Korolyuk, O. (2023). Hereditary hyperbilirubinemias: diagnostic approach and management. Lecture for postgraduate medical students. The Practitioner, (4), 88-92. Retrieved from https://plr.com.ua/index.php/journal/article/view/784

Abstract

Hyperbilirubinemia appears as jaundice or icterus, which can usually be detected when the serum bilirubin level exceeds 34 μmol/L. There are different types of predominantly unconjugated and predominantly conjugated bilirubinemias. Diagnostic approach to patients with icterus or hyperbilirubinemia was proposed. Clinical presentation, diagnostic criteria
and principles of treatment are described for Gilbert syndrome, Crigler-Najjar syndrome, Dubin-Johnson Syndrome and Rotor syndrome. Conclusion: benign hyperbilirubinemias are rare syndromes but can be distinguished from other liver injures with difficulties.

pdf (Українська)

References

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