A case report: Familial glucocorticoid deficiency associated with familial focal segmental glomerulosclerosis

BACKGROUND: Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder characterized by isolated glucocorticoid deficiency in the presence of normal plasma renin and aldosterone level. Focal segmental glomerulosclerosis (FSGS) is a form of glomerular disease associated with prot...

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Detalles Bibliográficos
Autores principales: Ram, Nanik, Asghar, Ali, Islam, Najmul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538046/
https://www.ncbi.nlm.nih.gov/pubmed/23232022
http://dx.doi.org/10.1186/1472-6823-12-32

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538046/
https://www.ncbi.nlm.nih.gov/pubmed/23232022
http://dx.doi.org/10.1186/1472-6823-12-32

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