Results 221 to 230 of about 37,111 (253)
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Pregnancies associated with primary adrenal insufficiency
Fertility and Sterility, 2008To provide a framework for the clinical presentation, evolution, treatment, and outcome of the unusual association between primary adrenal insufficiency (AI) during pregnancy and life-threatening complications for the mother and fetus.Case reports.Pregnant women with AI treated in the Endocrine and Diabetes Department, Hospital Universitario de ...
Carolina, Fux Otta +3 more
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Pathogenesis of primary adrenal insufficiency
Best Practice & Research Clinical Endocrinology & Metabolism, 2009Autoimmune Addison's disease is caused by autoreactivity towards the adrenal cortex involving 21-hydroxylase autoantibodies and autoreactive T cells. Autoimmune destruction of the adrenal cortex is triggered by hitherto unknown environmental factors in individuals with genetic susceptibility.
Eystein, Husebye, Kristian, Løvås
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Clinical Medicine (Russian Journal)
Due to the non-specificity of a number of clinical manifestations of Addison’s disease, the diagnosis of primary adrenal insufficiency in general therapeutic profile hospitals causes certain difficulties. The article presents a clinical case of diagnosing primary adrenal insufficiency in combination with autoimmune thyroiditis and hypogonadism as a ...
T. I. Kalenchits +3 more
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Due to the non-specificity of a number of clinical manifestations of Addison’s disease, the diagnosis of primary adrenal insufficiency in general therapeutic profile hospitals causes certain difficulties. The article presents a clinical case of diagnosing primary adrenal insufficiency in combination with autoimmune thyroiditis and hypogonadism as a ...
T. I. Kalenchits +3 more
openaire +2 more sources
Primary Adrenal Insufficiency and Hyperpigmentation
The American Journal of Medicine, 2023Manidipa Majumder +2 more
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The expanding world of primary adrenal insufficiencies
European Journal of Endocrinology, 1997The past few years have seen a phenomenal increase in our understanding of three genetic causes of primary adrenal and gonadal hormone deficiency. Lin and coworkers reported in 1995 (1) that patients with congenital lipoid adrenal hyperplasia have mutations of the steroidogenic acute regulatory protein.
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Adrenal hypoplasia congenita – an uncommon reason of primary adrenal insufficiency
Annales d'Endocrinologie, 2010Adrenal hypoplasia congenita (AHC) is a rare inherited condition characterised by primary adrenal failure and hypogonadotropic hypogonadism. Most cases arise from mutations in the NR0B1 gene (Xp21.3), which encodes an orphan nuclear receptor DAX-1. A 20-year-old patient was recently diagnosed with AHC.
M, Fichna +4 more
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