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Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in adolescence. Report of three siblings
BACKGROUND: Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder characterized by glucocorticoid deficiency, high ACTH levels and normal mineralocorticoid levels. FGD is caused due to defects in adrenocorticotropic hormone (ACTH) signaling. The defect can be caused by muta...
में बचाया:
| मुख्य लेखकों: | , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Medknow Publications & Media Pvt Ltd
2012
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3603085/ https://ncbi.nlm.nih.gov/pubmed/23565437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.104101 |
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