Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p

Bartter syndrome (BS) is a family of disorders manifested by hypokalemic hypochloremic metabolic alkalosis with normotensive hyperreninemic hyperaldosteronism. We evaluated a unique, inbred Bedouin kindred in which sensorineural deafness (SND) cosegregates with an infantile variant of the BS phenoty...

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Veröffentlicht in:	American journal of human genetics 1998-02, Vol.62 (2), p.355-361
Hauptverfasser:	Brennan, Theresa M.H., Landau, Daniel, Shalev, Hana, Lamb, Fred, Schutte, Brian C., Walder, Roxanne Y., Mark, Allyn L., Carmi, Rivka, Sheffield, Val C.
Format:	Artikel
Sprache:	eng
Schlagworte:	Bartter syndrome Bartter Syndrome - genetics Biological and medical sciences Chromosome 1 Chromosome Mapping Chromosomes, Human, Pair 1 Deafness Deafness - genetics DNA Primers Family Female Genetic Linkage Genetic Markers Genotype Glomerulonephritis Humans Linkage Male Medical sciences Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Pedigree Repetitive Sequences, Nucleic Acid Sensorineural deafness Tropical medicine
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