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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Shivaprasad, K. S., Dutta, Deep, Jain, Rajesh, Ghosh, Sujoy, Mukhopadhyay, Satinath, Chowdhury, Subhankar
Format: Artigo
Sprache:Inglês
Veröffentlicht: Medknow Publications & Media Pvt Ltd 2012
Schlagworte:
Brief Communication
Online Zugang: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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