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358 Possible Causes for Hyperaldosteronism, Polyuria

  • Endocrine Dysfunction

    Thyroid disease, hyperaldosteronism and hypomagnesaemia were uncommon but were probably not looked for in many cases.[] The common initial symptoms and signs included polyuria, polydipsia, rapid growth, neurologic deficit,sexual precocity, and growth retardation.[] A casual blood glucose greater than 200 mg/dL with associated symptoms such as polyuria, polydipsia, or unexplained weight loss is diagnostic of diabetes mellitus.[]

  • Adrenal Insufficiency

    Related : Adrenal Conditions Adrenocortical Carcinoma Adrenal Crisis CT Scan Cushing's Endoscopic Hyperaldosteronism Insufficiency Laparoscopic Pheochromocytoma Scar Gallery[] Over the next few days, however, the patient developed severe thirst and polyuria exceeding 6 L of urine per day, accompanied by hypernatraemia and hypo-osmolar urine.[] E26.81 Bartter's syndrome E26.89 Other hyperaldosteronism E26.9 Hyperaldosteronism, unspecified E27 Other disorders of adrenal gland E27.0 Other adrenocortical overactivity[]

  • Conn Syndrome

    How is Primary Hyperaldosteronism treated The treatment of primary hyperaldosteronism depends on the cause.[] […] pri·mar·y al·dos·ter·on·ism an adrenocortical disorder caused by excessive secretion of aldosterone and characterized by headaches, nocturia, polyuria, fatigue, hypertension[] It is often symptomless, but may present with symptoms of hypokalaemia – such as muscle weakness, fatigue, polyuria, cramps. 2/3 are due to a solitary mineralocorticoid producing[]

  • Bartter's Disease

    E26.0 Primary hyperaldosteronism E26.02 Glucocorticoid-remediable aldosteronism E26.09 Other primary hyperaldosteronism E26.1 Secondary hyperaldosteronism E26.8 Other hyperaldosteronism[] Abstract Bartter syndrome is an autosomic recessive disease characterized by severe polyuria and sodium renal loss.[] After birth he displayed extreme polyuria, severe renal sodium and chloride loss, and marked hypercalciuria.[]

  • Renal Tubular Acidosis

    . - child with hyperaldosteronism, hyperkalemia, metabolic acidosis, salt wasting, and hypotension. 2.[] Despite polyuria, both patients developed resistant hyperkalemia that needed further hemodialysis.[] Clinical Manifestations In children the clinical spectrum is nonspecific including anorexia, failure to thrive, vomiting and dehydration, constipation, polyuria, and polydipsia[]

  • Fanconi Syndrome

    The combination hypo/normotension, high serum renin and high serum aldosterone suggested secondary hyperaldosteronism.[] We discuss in this article the atypical electrolytes losses found in our patient, as well as the possible mechanisms of severe polyuria.[] These patients presented with a history of polydipsia, polyuria, weight loss, anorexia, and wasting. Interestingly, 1 patient was not taking protease inhibitors.[]

  • Loop Diuretic

    In fact, most sodium not reabsorbed in Henle's loop, due to the action of furosemide, is subsequently taken up in the distal nephron because of hyperaldosteronism.[] Fatigue, muscle weakness, leg cramps NV, paralytic ileus Soft, flabby muscles Paresthesias, decreased reflexes Weak, irregular pulse Polyuria, hyperglycemia What are 5 key[] In fact, most sodium not reabsorbed in Henle's loop, due to the action of furosemide , is subsequently taken up in the distal nephron because of hyperaldosteronism.[]

  • Autosomal Dominant Polycystic Kidney Disease

    Therefore, a rapid postoperative decline in eGFR was most likely due to correction of hyperaldosteronism.[] Higher concentrations of tolvaptan were less well tolerated, resulting in adverse events of pollakiuria, thirst, polyuria, nocturia, and a higher number of times out of bed[] The main side effects are marked polyuria and, in rare cases, liver toxicity.[]

  • Nephrocalcinosis

    Primary hyperaldosteronism is reported to facilitate urinary calcium excretion; however, renal calculi or calcinosis in this disorder has been rarely reported.[] In both cases, the profuse diarrhea, initially mistaken for polyuria, promptly resolved after the introduction of glucose-galactose-free milk.[] Osteoporosis due to immobilization, menopause, aging, or steroids Primary (familial) hyperoxaluria , or secondary hyperoxaluria Chronic disorders such as Bartter syndrome , primary hyperaldosteronism[]

  • Hypokalemia

    […] secondary hyperaldosteronism causes, and chondrocalcinosis.[] Genitourinary Polyuria or sexual dysfunction. [2] Medical Management (current best evidence) Severe hypokalmeia levels that cause ECG changes such as T-wave flattening or[] Rhabdomyolysis presenting with severe hypokalemia as the first manifestation of primary hyperaldosteronism is extremely rare.[]

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