Interleukin‐6 and cancer‐related hypoaldosteronism
نویسندگان
چکیده
منابع مشابه
Congenital hypoaldosteronism.
Congenital hypoaldosteronism due to an isolated aldosterone biosynthesis defect is rare. We report a 4 month old female infant who presented with failure to thrive, persistent hyponatremia and hyperkalemia. Investigations revealed normal serum 17 hydroxy progesterone and cortisol. A decreased serum aldosterone and serum 18 hydroxy corticosterone levels with a low 18 hydroxy corticosterone: aldo...
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long term benefit apparently due to chiropractic we initiated a three year follow up, sending multiple reminders to those initially not responding. By mid April 1990-beyond the closing date for the earlier resultsdata were available for 113 patients, representing a 79% response. At three years the mean fall in Oswestry score for those treated by chiropractic was 9-6% points more than for those ...
متن کاملHyperreninaemic hypoaldosteronism in a dog.
A 9-year-old male German shepherd dog was evaluated for clinical and clinico-pathological changes that were suggestive of Addison's disease. On further investigation the basal plasma cortisol concentration was high, a normal cortisol response to ACTH stimulation occurred, plasma renin activity was elevated and low serum aldosterone concentration was present. A diagnosis of hyperreninaemic hypoa...
متن کاملCyclosporin A-Induced Hyperreninemic Hypoaldosteronism
We studied the effects of cyclosporin A on the renin-aldosterone axis in SpragueDawley rats. Two weeks of intragastric administration of cyclosporin A (5 mg/kg/day or 20 mg/kg/day) resulted in large increases in plasma renin concentration (23 ± 5, 70 ±12, and 79 ± 11 ng/ml/hr in control rats and rats receiving 5 mg and 20 mg of cyclosporin A, respectively), with no parallel increments in plasma...
متن کاملMaternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.
Maternally-inherited diabetes with deafness (MIDD) is a rare form of monogenic diabetes that results, in most cases, from an A-to-G transition at position 3243 of mitochondrial DNA (m.3243A>G) in the mitochondrial-encoded tRNA leucine (UUA/G) gene. As the name suggests, this condition is characterized by maternally-inherited diabetes and bilateral neurosensory hearing impairment. A characterist...
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 1997
ISSN: 0361-8609,1096-8652
DOI: 10.1002/(sici)1096-8652(199702)54:2<171::aid-ajh15>3.3.co;2-3