Literature DB >> 8786597

Bartter's syndrome associated with severe retinopathy and presenting as pseudohypoaldosteronism in a newborn.

S Eckhardt1, M J Dillon, D B Grant.   

Abstract

Various pathophysiological explanations for Bartter's syndrome have been put forward since the condition was first described in 1962. It is currently thought that reduced reabsorption of sodium chloride in the distal tubule of the loop of Henle and the collecting ducts leads to secondary hyperkaluria and hypokalaemic metabolic alkalosis. We describe a 9 1/2-year-old boy with Bartter's syndrome and severe retinopathy whose features may be those of a previously unrecognized disorder.

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Year:  1995        PMID: 8786597      PMCID: PMC1295424     

Source DB:  PubMed          Journal:  J R Soc Med        ISSN: 0141-0768            Impact factor:   5.344


  4 in total

Review 1.  Bartter's syndrome: a unifying hypothesis.

Authors:  R Garrick; F N Ziyadeh; D Jorkasky; S Goldfarb
Journal:  Am J Nephrol       Date:  1985       Impact factor: 3.754

2.  The pathogenetic spectrum of Bartter's syndrome.

Authors:  J H Stein
Journal:  Kidney Int       Date:  1985-07       Impact factor: 10.612

3.  Erythrocyte sodium transport in Bartter's syndrome.

Authors:  M Uchiyama; V Shah; C Daman Willems; M J Dillon
Journal:  Acta Paediatr Scand       Date:  1988-11

4.  Oculocerebral hypopigmentation syndrome associated with Bartter syndrome.

Authors:  C P White; M Waldron; J E Jan; J E Carter
Journal:  Am J Med Genet       Date:  1993-06-15
  4 in total

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