Crigler Najjar Syndrome Type I, A Rare But Severe Cause Of Unconjugated Hyperbilirubinemia In Children

Journal Title: IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) - Year 2018, Vol 17, Issue 10

Abstract

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, can develop severe, permanent, unconjugated hyperbilirubinemia within the first few days of life resulting in chronic kernicterus.

Authors and Affiliations

Abebe Habtamu

Keywords

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  • EP ID EP401508
  • DOI -
  • Views 60
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How To Cite

Abebe Habtamu (2018). Crigler Najjar Syndrome Type I, A Rare But Severe Cause Of Unconjugated Hyperbilirubinemia In Children. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS), 17(10), 19-20. https://europub.co.uk./articles/-A-401508