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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...
में बचाया:
| मुख्य लेखकों: | , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Galenos Publishing
2010
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| विषय: | |
| ऑनलाइन पहुंच: | 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 |
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