Fainting Fanconi syndrome clarified by proxy: a case report

BACKGROUND: Rare diseases may elude diagnosis due to unfamiliarity of the treating physicians with the specific disorder. Yet, advances in genetics have tremendously enhanced our ability to establish specific and sometimes surprising diagnoses. CASE PRESENTATION: We report a case of renal Fanconi sy...

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Detalhes bibliográficos
Publicado no:BMC Nephrol
Main Authors: Walsh, Stephen Benedict, Unwin, Robert, Kleta, Robert, van’t Hoff, William, Bass, Paul, Hussain, Khalid, Ellard, Sian, Bockenhauer, Detlef
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5504823/
https://ncbi.nlm.nih.gov/pubmed/28693455
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-017-0649-8
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