Abstract
Bartter syndrome (BS) is one of the most well-known hereditary tubular disorders, characterized by hypokalemic, hypochloremic metabolic alkalosis, and polyuria/ polydipsia. This disease usually presents before or during infancy, and adult nephrologists often inherit the patients from pediatric nephrologists since this is a life-long condition. Here, a few case scenarios will be presented to recount how they first got diagnosed and how their clinical courses were during childhood until adulthood, in addition to a brief review of the disease and its treatment.
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Choi, N., & Kang, H. G. (2022). Bartter Syndrome: Perspectives of a Pediatric Nephrologist. Electrolyte and Blood Pressure. Korean Society of Electrolyte and Blood Pressure Research. https://doi.org/10.5049/EBP.2022.20.2.49
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