Literature DB >> 2940182

Bartter's syndrome and the atrial natriuretic factor gene.

R M Graham, K D Bloch, V B Delaney, E Bourke, J G Seidman.   

Abstract

We investigated whether the gene for atrial natriuretic factor, a recently discovered peptide hormone with potent natriuretic, diuretic, and vasorelaxant properties, was pathogenetically linked to an uncommon but well-defined fluid and electrolyte disorder, Bartter's syndrome. Restriction fragment length polymorphisms in the atrial natriuretic factor gene were sought in a large kindred with six of 23 family members being affected. A Bgl II polymorphism, identified in two of 40 (5%) apparently normal subjects, was found in one of two first-generation family members. This polymorphism was also present in five of seven unaffected second-generation siblings but in only three of six affected siblings. The failure of the absence or the presence of the polymorphism to cosegregate with the disease clearly indicates that in this kindred, the gene for atrial natriuretic factor is not linked to Bartter's syndrome.

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Year:  1986        PMID: 2940182     DOI: 10.1161/01.hyp.8.6.549

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  1 in total

1.  Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

Authors:  T M Brennan; D Landau; H Shalev; F Lamb; B C Schutte; R Y Walder; A L Mark; R Carmi; V C Sheffield
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

  1 in total

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