Familial Glucocorticoid Deficiency Type 2: A Case Report

Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disease resulting from resistance to the action of adrenocorticotropic hormone (ACTH) on the adrenal cortex, which leads to isolated glucocorticoid deficiency with normal mineralocorticoid secretion. It may present in infancy or...

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Detalles Bibliográficos
Autores principales: Akın, Leyla, Kurtoğlu, Selim, Kendirici, Mustafa, Akın, Mustafa Ali
Formato: Texto
Lenguaje:English
Publicado: Galenos Publishing 2010
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005676/
https://www.ncbi.nlm.nih.gov/pubmed/21274326
http://dx.doi.org/10.4274/jcrpe.v2i3.122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005676/
https://www.ncbi.nlm.nih.gov/pubmed/21274326
http://dx.doi.org/10.4274/jcrpe.v2i3.122

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