نتایج جستجو برای: addison disease
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BACKGROUND Mitochondrial diseases are a group of disorders caused by mutations in nuclear DNA or mitochondrial DNA, usually involving multiple organ systems. Primary adrenal insufficiency due to mitochondrial disease is extremely infrequent and has been reported in association with mitochondrial DNA deletion syndromes such as Kearns-Sayre syndrome. AIM To report a 3-year-old boy with Addison ...
Laugier-Hunziker syndrome is a rare, hereditary pigmentary disorder characterized by mucocutaneous lentiginous lesions and melanonychia. The condition regarded as benign since underlying malignancies or systemic disorders were not reported. Since various malignancy syndromes including Peutz-Jeghers Cronkhite-Canada cause of hyperpigmentation such Addison disease drugs are presented with similar...
The sixth author’s name is incorrect. The correct name is: The Swedish Addision Registry Study Group. The correct citation is: Mitchell AL, Bøe Wolff A, MacArthur K, Weaver JU, Vaidya B, The Swedish Addison Registry Study Group, et al. (2015) Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus. PLoS ONE 10(6): e0123550. doi:10.1371/journal.pone.012...
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