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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...
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| Main Authors: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2012
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| Fag: | |
| Online adgang: | 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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