نتایج جستجو برای: adrenal insufficiency

تعداد نتایج: 151338  

Journal: :Srpski arhiv za celokupno lekarstvo 2014
Jasmina Durković Tatjana Milenković Nils Krone Silvia Parajes Bojana Mandić

INTRODUCTION X-linked adrenal hypoplasia congenita (AHC) is a rare cause of adrenocortical insufficiency. Early postnatal diagnosis may prevent severe hypoglycemia, Addisonian crises and death. Low maternal estriol (E3) levels in the second trimester of pregnancy could indicate the possibility that the fetus suffers from a disorder that causes adrenal insufficiency. Suspicion is based on the fa...

2016
Olivia S. Edgar Angela K. Lucas-Herald Mohamad Guftar Shaikh

PURPOSE Prader Willi syndrome (PWS) is a rare genetic condition that has concurrent endocrinological insufficiencies. The presence of growth hormone deficiency has been well documented, but adrenal insufficiency (AI) is not widely reported. A review was conducted to investigate its prevalence and relevance in PWS in both adults and children. METHODOLOGY A literature review was performed with ...

2013
Yvan Jamilloux Eric Liozon Gregory Pugnet Sylvie Nadalon Kim Heang Ly Stephanie Dumonteil Guillaume Gondran Anne-Laure Fauchais Elisabeth Vidal

OBJECTIVES Giant cell arteritis (GCA) is a chronic systemic vasculitis of large and medium-sized arteries, for which long-term glucocorticoid (GC) treatment is needed. During GC withdrawal patients can suffer adrenal insufficiency. We sought to determine the time until recovery of adrenal function after long-term GC therapy, and to assess the prevalence and predictors for secondary adrenal insu...

Journal: :Vojnosanitetski pregled 2012
Radoslav Pejin Edita Stokić Mile Novković Sofija Banić-Horvat Milan Cvijanović

INTRODUCTION Autoimmune polyglandular syndrome type 2 is defined as adrenal insufficiency associated with autoimmune primary hypothyroidism and/or with autoimmune type 1 diabetes mellitus, but very rare vith myasthenia gravis. CASE REPORT We presented a case of an autoimmune polyglandular syndrome, type 2 associated with myasthenia gravis. A 49-year-old female with symptoms of muscle weakness...

ژورنال: یافته 2011
طایی, نادره, طرهانی, فریبا, عباسی, فرزانه,

Allgrove (AAA) syndrome or familial glucocorticoid deficiency or Tripple A Syndrome is a rare genetic disorder with transmitted autosomal recessive. Allgrove and colleagues first described this syndrome in 1978. Allgrove Syndrome characterized by Adrenal insufficiency, Alacrima and Achalasia. Neurological and dermatological findings may be presented in some patients. Hyperpigmentation and A...

AHMAD MOORAKl, BAHAR BASTANI, REZA ROFOUGARAN,

We report the case of a 65 year old man with recent onset of insulin requiring diabetes mellitus, frequent attacks of anginal chest pain, paroxysmal hypertension poorly controlled with three medications, hyperlipidemia, and mild renal insufficiency. The patient was found to have pheochromocytoma of the left adrenal gland, resection of which resulted in total resolution of diabetes, hyperte...

Journal: :Journal of veterinary internal medicine 2007
Jamie M Burkitt Steve C Haskins Richard W Nelson Philip H Kass

BACKGROUND A syndrome of relative adrenal insufficiency has been identified in septic humans, and is associated with hypotension and death. Relative adrenal insufficiency is generally associated with basal serum cortisol concentration within or above the reference range and a blunted cortisol response to adrenocorticotropic hormone administration. It is unknown whether relative adrenal insuffic...

Journal: :Turkish Journal of Endocrinology and Metabolism 2017

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