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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Hlavní autoři: Shivaprasad, K. S., Dutta, Deep, Jain, Rajesh, Ghosh, Sujoy, Mukhopadhyay, Satinath, Chowdhury, Subhankar
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2012
Témata:
Brief Communication
On-line přístup: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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