Renal Function in Patients with Addison's Disease and in Patients with Adrenal Insufficiency Secondary to Pituitary Pan-hypofunction.
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چکیده
منابع مشابه
Autoimmunity as the most frequent cause of idiopathic secondary adrenal insufficiency: report of 111 cases.
The origin of the isolated secondary adrenal insufficiency is unknown in most cases. An observation of a group of over 100 patients with secondary adrenal insufficiency and coexisting autoimmune abnormalities suggests that autoimmunity could be a frequent cause of idiopathic secondary failure, similarly as in Addison's disease. We studied 176 patients with idiopathic isolated secondary adrenal ...
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OBJECTIVE Addison's disease is frequently a component of autoimmune polyendocrinopathies while secondary adrenal insufficiency associated with autoimmune disorders is believed to be a rare event. We present a series of patients with secondary adrenal insufficiency coexisting with autoimmune diseases and/or antithyroid autoantibodies. DESIGN AND PATIENTS Among a group of 102 patients with seco...
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The possibility that papilloedema may occur in Addison's disease other than as a chance coincidence is not widely known. It has been possible to trace two accounts, both published since 1950, where this has been noted. This article provides an account of a third, very similar, case and also reports gross cerebral oedema in two other patients with adrenal insufficiency. Of these two patients, on...
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Idiopathic intracranial hypertension is a diagnosis of exclusion defined by elevated intracranial pressure without mass lesions or hydrocephalus. Causes of idiopathic intracranial hypertension include obesity, vitamin derangements, antibiotics, corticosteroids, and autoimmune disorders. Cushing's disease and Addison's disease have been associated with idiopathic intracranial hypertension. Secon...
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Sagliker syndrome is a rare form of renal osteodystrophy resulted from untreated secondary hyperparathyroidism. It is described by severe skeletal deformities, high level of PTH in patients with chronic renal failure, and deformed face. This paper reports a 44-year-old male patient with the mentioned characteristics. In addition to the unique clinical features, high levels of ALP and PTH hormon...
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عنوان ژورنال:
- The Journal of clinical investigation
دوره 21 1 شماره
صفحات -
تاریخ انتشار 1942