@article{oai:twinkle.repo.nii.ac.jp:00020179,
 author = {溝口, 由美子 and 鈴木, 里香 and 鈴木, 恵子 and 杉原, 茂孝},
 issue = {Extra},
 journal = {東京女子医科大学雑誌},
 month = {May},
 note = {東京女子医科大学東医療センター小児科開局40周年記念論文集, Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male patient admitted to our ward with hepatitis. His growth was severely retarded, and he had abnormalities of serum electrolytes including hyponatremia, hypokalemia, and hypochloremia with metabolic alkalosis. He needed continuous intravenous infusion and electrolyte supplementation. Further, his plasma renin and aldosterone concentrations were remarkably elevated. Because of his normal blood pressure, normal serum magnesium and hypercalciuria, we diagnosed him as having Bartter's syndrome. Gene analysis revealed type III Bartter's syndrome.},
 pages = {E85--E91},
 title = {著明な発育障害と血清電解質異常で発見されたBartter症候群の1例(東京女子医科大学東医療センター小児科開局40周年記念論文集)},
 volume = {77},
 year = {2007}
}