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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Detalles Bibliográficos
Autores principales: Walsh, Stephen Benedict, Unwin, Robert, Kleta, Robert, van’t Hoff, William, Bass, Paul, Hussain, Khalid, Ellard, Sian, Bockenhauer, Detlef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504823/
https://www.ncbi.nlm.nih.gov/pubmed/28693455
http://dx.doi.org/10.1186/s12882-017-0649-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504823/
https://www.ncbi.nlm.nih.gov/pubmed/28693455
http://dx.doi.org/10.1186/s12882-017-0649-8

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