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Literature DB >> 27408019

Bartter's Syndrome Masquerading as a Neurometabolic Disorder.

H R Ramamurthy¹, M Kanitkar², U Raju³.

Abstract

Entities: Disease

Keywords: Hyperreninism; Hypokalemia; Metabolic alkalosis

Year: 2011 PMID： 27408019 PMCID： PMC4922377 DOI： 10.1016/S0377-1237(07)80157-2

Source DB: PubMed Journal: Med J Armed Forces India ISSN： 0377-1237

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References

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9 in total

1. Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.

Authors: N Jeck; S C Reinalter; T Henne; W Marg; R Mallmann; K Pasel; M Vollmer; G Klaus; A Leonhardt; H W Seyberth; M Konrad
Journal: Pediatrics Date: 2001-07 Impact factor: 7.124

2. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome.

Authors: F C BARTTER; P PRONOVE; J R GILL; R C MACCARDLE
Journal: Am J Med Date: 1962-12 Impact factor: 4.965

3. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Authors: D B Simon; R S Bindra; T A Mansfield; C Nelson-Williams; E Mendonca; R Stone; S Schurman; A Nayir; H Alpay; A Bakkaloglu; J Rodriguez-Soriano; J M Morales; S A Sanjad; C M Taylor; D Pilz; A Brem; H Trachtman; W Griswold; G A Richard; E John; R P Lifton
Journal: Nat Genet Date: 1997-10 Impact factor: 38.330

Review 9. Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis.

Authors: A Bettinelli; G Vezzoli; G Colussi; M G Bianchetti; F Sereni; G Casari
Journal: J Nephrol Date: 1998 Mar-Apr Impact factor: 3.902

9 in total

Bartter's Syndrome Masquerading as a Neurometabolic Disorder.

1. Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.

2. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome.

3. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

4. Bartter syndrome in Costa Rica: a description of 20 cases.

5. Neonatal Bartter syndrome.

6. Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter disease.

7. Hypokalemic respiratory paralysis in Bartter's syndrome.

8. "Neonatal variant" of Bartter syndrome presenting with acidosis.

Review 9. Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis.