Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families

Adv Nephrol Necker Hosp. 2001:31:55-68.

Authors

S Disse-Nicodème, J M Achard, J Potier, M Delahousse, B Fiquet-Kempf, N Stern, A Blanchard, J C Guilbaud, P Niaudet, D Chauveau, B Dussol, Y Berland, P Dequiedt, J L Ader, M Paillard, J P Grünfeld, A Fournier, P Corvol, X Jeunemaitre

PMID: 11692471

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Adult
Family Health
Female
Genes, Dominant
Genetic Heterogeneity
Humans
Hyperkalemia / diagnosis
Hyperkalemia / genetics*
Hypertension / diagnosis
Hypertension / genetics*
Male
Middle Aged
Pedigree
Phenotype
Pseudohypoaldosteronism / diagnosis
Pseudohypoaldosteronism / genetics*