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...

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Detaylı Bibliyografya
Yayımlandı:J Med Case Rep
Asıl Yazarlar: Piloya, Thereza, Ssematala, Hawa, Dramani, Lydia Paparu, Nalikka, Oliva, Baluka, Miriam, Musiime, Victor
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7526154/
https://ncbi.nlm.nih.gov/pubmed/32993803
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-020-02488-5
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