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Fanconi–Bickel syndrome in a Ugandan child – diagnostic challenges in resource-limited settings: a case report
BACKGROUND: Fanconi–Bickel syndrome is an autosomal recessive disorder of glucose metabolism. It is an extremely rare disorder. Most cases have been reported in consanguineous communities. None of the cases have been reported in Black Africans in sub-Saharan Africa. This case was diagnosed 3 years a...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526154/ https://www.ncbi.nlm.nih.gov/pubmed/32993803 http://dx.doi.org/10.1186/s13256-020-02488-5 |