- Heterozygous Mutations of The Gene for Kir 1.1 (ROMK) in Antenatal Bartter Syndrome Presenting with Transient Hyperkalemia, Evolving to a Benign Course
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Cho JT, Guay-Woodford LM
- KMID: 1099795
- J Korean Med Sci.
- 2003 Feb;18(1):65-68.
- doi: 10.3346/jkms.2003.18.1.65
Bartter-like syndrome encompasses a set of inherited renal tubular disorders associated with hypokalemic metabolic alkalosis, renal salt wasting, hyperreninemic hyperaldosteronism, and normal blood pressure. Antenatal Bartter syndrome, a subtype of... -
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