A rare cause of refractory severe polyhydramnios: Antenatal bartter syndrome

Gina Nam, Angela Cho, Mi Hye Park

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Background: Antenatal Bartter syndrome is an autosomal recessive disorder causing severe polyuria that leads to severe polyhydramnios and preterm labor. Prenatal diagnosis of antenatal Bartter syndrome is difficult because the genetic diagnosis can only be confirmed following a clinical diagnosis in infants. Reports of prenatal diagnosis and treatment of antenatal Bartter syndrome are limited. Case Presentation: We present the case of a 33-year-old pregnant woman with refractory poly-hydramnios at 31 weeks of gestation. There were no structural anomalies or placental problems on ultrasonography; therefore, antenatal Bartter syndrome was suspected. With repeated amniocentesis and indomethacin therapy, the pregnancy continued to 36 weeks of gestation. The clinical features of the infant and subsequent genetic testing confirmed the diagnosis of antenatal Bartter syndrome. The baby was in good clinical condition at the 3-month follow-up visit. Conclusions: For pregnant women with early onset and refractory severe polyhydramnios without morphological anomalies, antenatal Bartter syndrome should be highly suspected.

Original languageEnglish
Article number272
JournalMedicina (Lithuania)
Volume57
Issue number3
DOIs
StatePublished - 2021

Bibliographical note

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • Amniotic fluid
  • Antenatal Bartter syndrome
  • Indomethacin
  • Polyhydramnios

Fingerprint

Dive into the research topics of 'A rare cause of refractory severe polyhydramnios: Antenatal bartter syndrome'. Together they form a unique fingerprint.

Cite this