Literature DB >> 1788991

Pseudohypoaldosteronism: case report and discussion of the syndrome.

D C Throckmorton1, M J Bia.   

Abstract

A 41-year-old man, complaining of leg cramps, was found to have persistent hyperkalemia. Except for mild hypertension, his physical examination and laboratory values to exclude connective tissue diseases and diabetes mellitus were normal. Renal function testing revealed a normal glomerular filtration rate and tubular capacity to acidify and dilute, as well as near-normal ability to concentrate his urine. Hormonal evaluation revealed a normal cortisol, as well as normal resting and stimulated renin and aldosterone levels. A selective defect in tubular potassium secretion was demonstrated. In the absence of aldosterone deficiency or renal dysfunction, it was assumed that the patient had primary renal resistance to aldosterone, known as pseudohypoaldosteronism. Treatment with hydrochlorothiazide controlled his hyperkalemia and hypertension. His case emphasizes the diagnostic and therapeutic factors that should be considered in evaluating and treating a non-hospitalized patient with sustained hyperkalemia.

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Year:  1991        PMID: 1788991      PMCID: PMC2589321     

Source DB:  PubMed          Journal:  Yale J Biol Med        ISSN: 0044-0086


  29 in total

1.  Pseudohypo-adrenalocorticism; renal sodium loss, hyponatremia, and hyperkalemia due to a renal tubular insensitivity to mineralocorticoids.

Authors:  G N DONNELL; N LITMAN; M ROLDAN
Journal:  AMA J Dis Child       Date:  1959-06

2.  A salt-losing syndrome in infancy. Pseudo-hypoadrenocorticalism.

Authors:  D N RAINE; J ROY
Journal:  Arch Dis Child       Date:  1962-10       Impact factor: 3.791

3.  A salt wasting syndrome in infancy.

Authors:  D B CHEEK; J W PERRY
Journal:  Arch Dis Child       Date:  1958-06       Impact factor: 3.791

4.  Familial pseudohypoaldosteronism.

Authors:  C Popow; A Pollak; K Herkner; S Scheibenreiter; W Swoboda
Journal:  Acta Paediatr Scand       Date:  1988-01

5.  Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiency.

Authors:  D Bosson; U Kuhnle; N Mees; J Ramet; E Vamos; F Vertongen; R Wolter; D Armanini
Journal:  Acta Endocrinol Suppl (Copenh)       Date:  1986

6.  Hyperkalemia in salt-wasting nephropathy. Study of the mechanism.

Authors:  M M Popovtzer; F H Katz; W F Pinggera; J Robinette; C G Halgrimson; D E Butkus
Journal:  Arch Intern Med       Date:  1973-08

7.  Hypertension and severe hyperkalaemia associated with suppression of renin and aldosterone and completely reversed by dietary sodium restriction.

Authors:  R D Gordon; R A Geddes; C G Pawsey; M W O'Halloran
Journal:  Australas Ann Med       Date:  1970-11

8.  Syndrome of idiopathic hyperkalaemia and hypertension with decreased plasma renin activity: effects on plasma renin and aldosterone of reducing the serum potassium level.

Authors:  G S Stokes; J L Gentle; K D Edwards; J H Stewart
Journal:  Med J Aust       Date:  1968-12-07       Impact factor: 7.738

9.  Hyperkalemia, hypertension and systemic acidosis without renal failure associated with a tubular defect in potassium excretion.

Authors:  J E Arnold; J K Healy
Journal:  Am J Med       Date:  1969-09       Impact factor: 4.965

10.  Aldosterone-receptor deficiency in pseudohypoaldosteronism.

Authors:  D Armanini; U Kuhnle; T Strasser; H Dorr; I Butenandt; P C Weber; J R Stockigt; P Pearce; J W Funder
Journal:  N Engl J Med       Date:  1985-11-07       Impact factor: 91.245

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