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Updated: Jul 2, 2026

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Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
Severe Polyhydramnios Associated With Antenatal Bartter Syndrome
Dynora Pierre-Louis1, Iliza Minaya1, Sohni Pathan1
1Obstetrics and Gynecology, HCA Healthcare, Margate, USA.
Cureus
|July 1, 2026
Summary
Severe polyhydramnios in a structurally normal fetus may indicate antenatal Bartter syndrome. Early recognition of this rare genetic disorder is crucial for improved neonatal outcomes and perinatal planning.
Area of Science:
- Perinatology
- Neonatology
- Medical Genetics
Background:
- Polyhydramnios, an excess of amniotic fluid, is typically diagnosed in the second or third trimester.
- While often idiopathic, it can be linked to maternal, fetal, or genetic conditions.
- Severe cases necessitate thorough investigation into underlying causes.
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