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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Akın, Leyla, Kurtoğlu, Selim, Kendirici, Mustafa, Akın, Mustafa Ali
Format: Artigo
Jezik:Inglês
Izdano: Galenos Publishing 2010
Teme:
Case Reports
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3005676/
https://ncbi.nlm.nih.gov/pubmed/21274326
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.v2i3.122
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki