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Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature

BACKGROUND: Fanconi–Bickel syndrome (FBS) is a rare autosomal recessive disorder caused by mutation of the SLC2A2 gene, which encodes glucose transporter protein 2 (GLUT2). CASE SUMMARY: We report a 7-mo-old girl with cytomegalovirus infection presenting hepatomegaly, jaundice, liver transaminase el...

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Detalles Bibliográficos
Autores principales:	Xiong, Li-Jing, Jiang, Mao-Ling, Du, Li-Na, Yuan, Lan, Xie, Xiao-Li
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Baishideng Publishing Group Inc 2020
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674741/ https://www.ncbi.nlm.nih.gov/pubmed/33269285 http://dx.doi.org/10.12998/wjcc.v8.i21.5467

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