Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone
Abstract
Objective Bartter syndrome is a severe inherited tubulopathy characterized by postnatal salt wasting, severe polyuria, dehydration, failure to thrive and secondary hyperaldosteronism. Prenatally, the disease is usually discovered following the onset of severe polyhydramnios in the second trimester. We studied amniotic fluid aldosterone concentration in Bartter syndrome and in controls. Methods Amniotic fluid aldosterone was assayed by...
Paper Details
Title
Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone
Published Date
Dec 1, 2015
Journal
Volume
36
Issue
1
Pages
88 - 91
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