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pubmed-article:10419618pubmed:abstractTextBartter syndrome is characterized by renal potassium and chloride loss, hypokalaemia, hypochloraemic metabolic alkalosis and increased plasma renin activity along with elevated angiotensin II and hyperaldosteronism. For diagnosis we conducted biochemical examinations of both amniotic fluid and the mother's urine. Except for potassium, amniotic fluid electrolytes in a mother with a fetus with Bartter syndrome were high. Urinary chloride, sodium and calcium were very low. Thus, the latter parameters may allow prediction of fetal Bartter syndrome during the prenatal period.lld:pubmed
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pubmed-article:10419618pubmed:authorpubmed-author:SuzukiYYlld:pubmed
pubmed-article:10419618pubmed:authorpubmed-author:MatsushitaYYlld:pubmed
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pubmed-article:10419618pubmed:copyrightInfoCopyright 1999 John Wiley & Sons, Ltd.lld:pubmed
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pubmed-article:10419618pubmed:volume19lld:pubmed
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pubmed-article:10419618pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:10419618pubmed:articleTitleBiochemical examination of mother's urine is useful for prenatal diagnosis of Bartter syndrome.lld:pubmed
pubmed-article:10419618pubmed:affiliationDepartment of Obstetrics and Gynaecology, Nagoya City University Medical School, Nagoya, Japan.lld:pubmed
pubmed-article:10419618pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10419618pubmed:publicationTypeCase Reportslld:pubmed