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Transient Pseudohypoaldosteronism in a 5-Month-old Infant Manifested as a Failure to Thrive

Lee JW, Cho SJ, Kim HS

Pseudohypoaldosteronism (PHA) in infants is manifested by presence of hyperkalemia, hyponatremia, and metabolic acidosis. At initial stages, PAH is generally suspected as congenital adrenal hyperplasia. Transient PHA has been reported...
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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes

Jeong HA, Park YK, Jung YS, Nam MH, Nam HK, Lee KH, Rhie YJ

Hyponatremia and hyperkalemia in infancy can be attributed to various causes, originating from a variety of renal and genetic disorders. Pseudohypoaldosteronism type 1 (PHA1) is one of these disorders, causing...
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Pseudohypoaldosteronism Type 1

Cheong HI

Pseudohypoaldosteronism (PHA), a rare syndrome of systemic or renal mineralocorticoid resistance, is clinically characterized by hyperkalemia, metabolic acidosis, and elevated plasma aldosterone levels with either renal salt wasting or hypertension....
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A Case of Autosomal Recessive Pseudohypoaldosteronism Type 1 with a Novel Mutation in the SCNN1A Gene

Kim SY, Lee JH, Cheong HI, Park YS

  • KMID: 2098923
  • J Korean Soc Pediatr Nephrol.
  • 2013 Oct;17(2):137-142.
Pseudohypoaldosteronism (PHA) is a condition characterized by renal salt wasting, hyperkalemia, and metabolic acidosis due to renal tubular resistance to aldosterone. Systemic PHA1 is a more severe condition caused by...
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A Case of Pseudohypoaldosteronism Type l Diagnosed after Infancy

Han SB, Lim CH, Lee KY, Kim JS, Kim WH, Uhm M

  • KMID: 2193470
  • J Korean Soc Pediatr Endocrinol.
  • 2007 Jun;12(1):82-86.
Pseudohypoaldosteronism (PHA) type l is a rare neonatal disease characterized by salt wasting, dehydration, hyperkalemia and metabolic acidosis. It is unresponsive to mineralocorticoid treatment with elevated aldosterone concentration. The three...
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A Case of Transient Pseudohypoaldosteronism Secondary to Ureteropelvic Junction Obstruction

Choi J, Hahn H, Park YS, You HW

  • KMID: 2197669
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):91-95.
We report a 2-month-old boy who presented with severe hyponatremia and hyperkalemia secondary to ureteropelvic junction(UPJ) obstruction. By prenatal ultrasonography at 19 weeks of gestation, severe hydronephrosis was found which...
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Two Cases with Pseudohypoaldosteronism

Kim SJ, Lim PJ, Ban SH, Lee DH, Jin DK, Song SM, Kim JS

  • KMID: 2001528
  • J Korean Soc Pediatr Endocrinol.
  • 2000 Dec;5(2):215-219.
Pseudohypoaldosteronism is a disorder in which synthesis of aldosterone is normal but unresponsiveness of the target to the aldosterone activates angiotensin-renin system which in turn elevates levels of renin and...
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A Case of Pseudohypoaldosteronism

Kang IN, Lee JW, Bang JG, Lee DB

  • KMID: 1662053
  • J Korean Pediatr Soc.
  • 1995 Aug;38(8):1160-1163.
No abstract available.
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Two Male Siblings with Pseudohypoaldosteronism Type I

Lee R, Kim SY, Choi SD, Chung SY, Kang JH, Lee BC

  • KMID: 2335095
  • J Korean Pediatr Soc.
  • 1994 Feb;37(2):262-268.
Pseudohypoaldosteronism (PHA) is rare herediary salt wasting syndrome due to peripheral resistance to aldostrone. PHA type I, subdivided into isolated renal insensitivity to aldosterone of autosomal dominant inheritance and multiple...
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Two Cases of Pseudohypoaldosteronism Type I

Lee JE, Seo JW, Lee SJ

  • KMID: 2142496
  • J Korean Pediatr Soc.
  • 1994 Jan;37(1):122-128.
Pseudohypoaldosteronism type 1 is a genetic renal tubular disease of salt wasting, presenting in young infants. Tubular unresponsiveness to elevated endogenous and exogenous aldosterone is the suggested pathogenetic mechanism. Oral...
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A case of pseudohypoaldosteronism

Kwon YS, Shin HG, Ahn MS, Kim HB

  • KMID: 1691103
  • J Korean Pediatr Soc.
  • 1992 Jul;35(7):984-988.
No abstract available.
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