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
Format: Artikel
Sprache:eng
Schlagworte:
Enzymes
Genetic disorders
Liver diseases
Medical diagnosis
Young adults
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Zusammenfassung: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
ISSN:1997-9797
2075-5384
DOI:10.3329/jom.v12i1.6359