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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Bibliografiske detaljer
Main Authors: Shivaprasad, K. S., Dutta, Deep, Jain, Rajesh, Ghosh, Sujoy, Mukhopadhyay, Satinath, Chowdhury, Subhankar
Format: Artigo
Sprog:Inglês
Udgivet: Medknow Publications & Media Pvt Ltd 2012
Fag:
Brief Communication
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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