- A case of pseudohypoaldosteronism
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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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- A Case of Pseudohypoaldosteronism
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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 Cases with Pseudohypoaldosteronism
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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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- Transient Pseudohypoaldosteronism in a 5-Month-old Infant Manifested as a Failure to Thrive
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Lee JW, Cho SJ, Kim HS
- KMID: 2433550
- Ewha Med J.
- 2019 Jan;42(1):6-9.
- doi: 10.12771/emj.2019.42.1.6
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 premature neonate with severe polyhydramnios in utero
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Ahn SY, Shin SM, Kim KA, Lee YK, Ko SY
- KMID: 2281118
- Korean J Pediatr.
- 2009 Mar;52(3):376-379.
- doi: 10.3345/kjp.2009.52.3.376
We report a case of a premature newborn baby who presented with hyponatremia, hyperkalemia, and metabolic acidosis accompanied by severe polyhydramnios in utero. The baby was diagnosed with pseudohypoaldosteronism on... -
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- Transient Pseudohypoaldosteronism in an Infant with Vesicoureteral Reflux
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Kim MK, Park SE, Lee JH
- KMID: 2144673
- J Korean Soc Pediatr Nephrol.
- 2012 Apr;16(1):54-57.
A 6-month-old boy with vesicoureteral reflux exhibited features of transient type 1 pseudohypoaldosteronism (PHA) in the course of urinary tract infection. PHA presents hyponatremia, hyperkalemia, and metabolic acidosis, accompanying with... -
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- Two Cases of Pseudohypoaldosteronism Type I
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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 Transient Pseudohypoaldosteronism Secondary to Ureteropelvic Junction Obstruction
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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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- A case of idiopathic renal hypouricemia
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Han MH, Park SU, Kim DS, Shim JW, Shim JY, Jung HL, Park MS
- KMID: 2072887
- Korean J Pediatr.
- 2007 May;50(5):489-492.
- doi: 10.3345/kjp.2007.50.5.489
Idiopathic renal hypouricemia is a disorder characterized by impaired urate handling in the renal tubules. This disease usually produces no symptoms, but hematuria, uric acid nephrolithiasis or acute renal failure... -
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- A Case of Autosomal Recessive Pseudohypoaldosteronism Type 1 with a Novel Mutation in the SCNN1A Gene
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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 1 with a mutation in the mineralocorticoid receptor gene
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Lee SE, Jung YH, Han KH, Lee HK, Kang HG, Ha IS, Choi Y, Cheong HI
- KMID: 2073627
- Korean J Pediatr.
- 2011 Feb;54(2):90-93.
- doi: 10.3345/kjp.2011.54.2.90
Pseudohypoaldosteronism type 1 (PHA1) is a rare form of mineralocorticoid resistance characterized in newborns by salt wasting with dehydration, hyperkalemia and failure to thrive. This disease is heterogeneous in etiology... -
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- A Case of Pseudohypoaldosteronism Type l Diagnosed after Infancy
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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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- Management of a 25-day-old Male Presenting with a First Episode of Acute Pyelonephritis, and Persistent Hyperkalemia with Normal Serum Aldosterone
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Kang YS, Choi JY, Lee JH
- KMID: 1733224
- J Korean Soc Pediatr Nephrol.
- 2014 Oct;18(2):111-115.
- doi: 10.3339/jkspn.2014.18.2.111
Hyperkalemia is often detected in young infants, particularly in association with acute pyelonephritis or a urinary tract anomaly. Cases of hyperkalemia in this population may also be due to transient... -
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- A Case of Type IV-4 Renal Tubular Acidosis
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Jo YA, Kim DU, Lee YK, Choi BJ, Kim JT, Lee IJ
- KMID: 2208070
- J Korean Pediatr Soc.
- 1997 Nov;40(11):1603-1607.
Type IV renal tubular acidosis (RTA) is due to renal tubular bicarbonate wasting associated with mineralocorticoid deficiency. In its five subtypes, IV-4 is due to pseudohypoaldosteronism (PHA) evidenced by increased... -
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- Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes
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Jeong HA, Park YK, Jung YS, Nam MH, Nam HK, Lee KH, Rhie YJ
- KMID: 2354701
- Ann Pediatr Endocrinol Metab.
- 2015 Dec;20(4):230-234.
- doi: 10.6065/apem.2015.20.4.230
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
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Cheong HI
- KMID: 1811001
- J Genet Med.
- 2013 Dec;10(2):81-87.
- doi: 10.5734/JGM.2013.10.2.81
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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- Two Male Siblings with Pseudohypoaldosteronism Type I
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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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- Heterozygous Mutations of The Gene for Kir 1.1 (ROMK) in Antenatal Bartter Syndrome Presenting with Transient Hyperkalemia, Evolving to a Benign Course
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Cho JT, Guay-Woodford LM
- KMID: 1099795
- J Korean Med Sci.
- 2003 Feb;18(1):65-68.
- doi: 10.3346/jkms.2003.18.1.65
Bartter-like syndrome encompasses a set of inherited renal tubular disorders associated with hypokalemic metabolic alkalosis, renal salt wasting, hyperreninemic hyperaldosteronism, and normal blood pressure. Antenatal Bartter syndrome, a subtype of... -
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- WNKs: protein kinases with a unique kinase domain
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Huang CL, Cha SK, Wang HR, Xie J, Cobb MH
- KMID: 1090959
- Exp Mol Med.
- 2007 Oct;39(5):565-573.
WNKs (with-no-lysine [K]) are a family of serine-threonine protein kinases with an atypical placement of the catalytic lysine relative to all other protein kinases. The roles of WNK kinases in... -
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