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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Materias: | |
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 |