نتایج جستجو برای: addison disease

تعداد نتایج: 1490684  

Journal: :acta medica iranica 0
hamdollah karamifar department of pediatric endocrinology and metabolism, school of medicine, shiraz university of medical sciences, fars, iran. satila dalili department of pediatric endocrinology and metabolism, school of medicine, shiraz university of medical sciences, fars, iran. zohreh karamizadeh department of pediatric endocrinology and metabolism, school of medicine, shiraz university of medical sciences, fars, iran. gholamhosein amirhakimi department of pediatric endocrinology and metabolism, school of medicine, shiraz university of medical sciences, fars, iran. hosein dalili department of pediatric endocrinology and metabolism, school of medicine, shiraz university of medical sciences, fars, iran.

autoimmune polyglandular syndrome (aps) type 2 is characterized by the presence of addison's disease, in association with autoimmune thyroid disease and/or type 1 diabetes mellitus. aps type 2 occurs most often in middle aged females and is rare in children. here an 11 year old boy is reported with addison's disease who developed symptom's of diabetes mellitus, goiter, malabsorption, macrocytic...

کرامت, فریبا,

Primary adernal insufficiency, the so-called Addision’d disease rarely and few cases have been reported due to tuberculosis. The case, a 55 years old man , complaining of severe malaise & anorexia, was admitted in 22 sept,1996. One week before admission, antituberculosis therapy had been started with a previous diagnosis of cervical lymphadenitis documented by pathologic examination of ...

Journal: :The Journal of clinical endocrinology and metabolism 2018
Daniel Eriksson Frida Dalin Gabriel Nordling Eriksson Nils Landegren Matteo Bianchi Åsa Hallgren Per Dahlqvist Jeanette Wahlberg Olov Ekwall Ola Winqvist Sergiu-Bogdan Catrina Johan Rönnelid Anna-Lena Hulting Kerstin Lindblad-Toh Mohammad Alimohammadi Eystein S Husebye Per Morten Knappskog Gerli Rosengren Pielberg Sophie Bensing Olle Kämpe

Context Autoimmune polyendocrine syndrome type 1 (APS1) is a monogenic disorder that features autoimmune Addison disease as a major component. Although APS1 accounts for only a small fraction of all patients with Addison disease, early identification of these individuals is vital to prevent the potentially lethal complications of APS1. Objective To determine whether available serological and ...

Journal: :The American Journal of the Medical Sciences 1871

Journal: :Indian pediatrics 2005
N Mehta P Parekh

skin, starting from face since the age of 4 years. There was history of recurrent episodes of loose motions, vomiting and fever after the age of 4 years in the elder sibling for which he was hospitalized in a state of shock. Family history, perinatal history and developmental history were non-contributory. General and systemic examinations were unremarkable except for the generalized hyperpigme...

Journal: :British medical journal 1975
L H Rees D B Grant J Wilson

Raised plasma immunoreactive corticotrophin (ACTH) levels were found in five boys with the sex-linked disorder progressive leucodystrophy associated with adrenal insufficiency (Addison-Schilder's disease) and in a symptom-free brother of one of them. Similar ACTH concentrations were found using two antisera, one against the N-terminal part of the ACTH molecule and the other against the C-termin...

Journal: :The Journal of Nervous and Mental Disease 1918

Journal: :American family physician 2014
Aaron Michels Nicole Michels

Primary adrenal insufficiency, or Addison disease, has many causes, the most common of which is autoimmune adrenalitis. Autoimmune adrenalitis results from destruction of the adrenal cortex, which leads to deficiencies in glucocorticoids, mineralocorticoids, and adrenal androgens. In the United States and Western Europe, the estimated prevalence of Addison disease is one in 20,000 persons; ther...

Hossein Assadian,

SUMMARY Three pa ticnts admitted because of slightly increased serum amino trans fcrases were found to have Addison's disease. A review of 16 other patients with addison 's disease who had serum aminotransferase activity (aspartate aminotrans­ferase (ASAT) and alanine aminotransferase (ALAT) J determined prior to treatment revealed one more patient with slightly increased aminotransferase acti...

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