Crigler-Najjar Syndrome Type 2 in a Young Adult

Crigler-Najjar Syndrome Type 2 in a Young Adult

Crigler-Najjar syndrome type 2 in an autosomal recessive congenital non-hemolytic hyperbilirubinemia caused by UDP-glucuronosyltransferase deficiency. Only a few hundred cases have been described in the literature so far. We are reporting Crigler-Najjar syndrome type 2 in an 18 year old female born...

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Veröffentlicht in:Journal of medicine 2011, Vol.12 (1), p.86-88
Hauptverfasser: Haque, Md. Azizul, Sharmin, Laila Shamima, Harun or Rashid, Mohd, Alim, MA, Ekram, ARM Saifuddin, Mowla, Syed Ghulam Mogni
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Enzymes
Genetic disorders
Liver diseases
Medical diagnosis
Young adults
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container_title Journal of medicine
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creator Haque, Md. Azizul
Sharmin, Laila Shamima
Harun or Rashid, Mohd
Alim, MA
Ekram, ARM Saifuddin
Mowla, Syed Ghulam Mogni
description Crigler-Najjar syndrome type 2 in an autosomal recessive congenital non-hemolytic hyperbilirubinemia caused by UDP-glucuronosyltransferase deficiency. Only a few hundred cases have been described in the literature so far. We are reporting Crigler-Najjar syndrome type 2 in an 18 year old female born out of consanguineous marriage. Keyword: Crigler-Najjar syndrome; UDP-glucuronosyltransferase; Bangladesh DOI: 10.3329/jom.v12i1.6359J Medicine 2011; 12 : 81-85
doi_str_mv 10.3329/jom.v12i1.6359
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source Bangladesh Journals Online; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Enzymes
Genetic disorders
Liver diseases
Medical diagnosis
Young adults
title Crigler-Najjar Syndrome Type 2 in a Young Adult
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