Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia

We experienced a case of a 19-year-old man with Gilbert syndrome with concomitant hereditary spherocytosis. The patient presented with moderate unconjugated hyperbilirubinemia, and inherited etiology was strongly suspected. The diagnosis of Gilbert syndrome was confirmed by the genetic analysis of t...

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Detalles Bibliográficos
Autores principales: Aiso, Mitsuhiko, Yagi, Minami, Tanaka, Atsushi, Miura, Kotaro, Miura, Ryo, Arizumi, Toshihiko, Takamori, Yoriyuki, Nakahara, Sayuri, Maruo, Yoshihiro, Takikawa, Hajime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410476/
https://www.ncbi.nlm.nih.gov/pubmed/28321066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410476/
https://www.ncbi.nlm.nih.gov/pubmed/28321066

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