Hereditary Spherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II

Patients with co-existing hereditary spherocytosis (HS) and UDP-glucuronosyltransferase 1A1 (UGT1A1) deficiency as Gilbert's syndrome (GS) have been reported, and previous studies have demonstrated an increased risk for developing gallstones in patients with co-inheritance of GS and HS. We expe...

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Detalles Bibliográficos
Autores principales: Iijima, Shigeo, Ohzeki, Takehiko, Maruo, Yoshihiro
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051216/
https://www.ncbi.nlm.nih.gov/pubmed/21319362
http://dx.doi.org/10.3349/ymj.2011.52.2.369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051216/
https://www.ncbi.nlm.nih.gov/pubmed/21319362
http://dx.doi.org/10.3349/ymj.2011.52.2.369

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