CRIGLER NAJJAR SYNDROME TYPE I, A RARE BUT SEVERE CAUSE OF UNCONJUGATED HYPERBILIRUBINEMIA IN CHILDREN
Abstract
Crigler Najjar Syndrome Type I is a rare and severe autosomal recessive disorder of bilirubin metabolism. It has been associated with consanguinity in some patients. Infants without any evidence of hemolysis, develop severe, permanent, unconjugated hyperbilirubinemia within the first few days of life resulting in chronic kernicterus
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Published
2018-12-21
How to Cite
Habtamu, A. (2018). CRIGLER NAJJAR SYNDROME TYPE I, A RARE BUT SEVERE CAUSE OF UNCONJUGATED HYPERBILIRUBINEMIA IN CHILDREN. Ethiopian Journal of Pediatrics and Child Health, 13(2). Retrieved from https://www.ejpch.net/index.php/ejpch/article/view/85
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Section
Case Report