Antenatal Bartter syndrome (Q85249): Difference between revisions
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dki-india-ID_1424120171 | |||||||||||||||
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13 August 2026
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Latest revision as of 10:36, 15 August 2026
This is a rare inherited defect characterised by polyhydramnios (Increased water in the uterus) due to polyuria in utero. In contrast to Classic Bartter Syndrome and Gitelman Syndrome, the Antenatal variant of Bartter Syndrome has both the features of metabolic alkalosis (from the low potassium), as well as profound systemic manifestations. Out of all of the variants, this form is the most severe.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1424120171 |
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| English | Antenatal Bartter syndrome |
This is a rare inherited defect characterised by polyhydramnios (Increased water in the uterus) due to polyuria in utero. In contrast to Classic Bartter Syndrome and Gitelman Syndrome, the Antenatal variant of Bartter Syndrome has both the features of metabolic alkalosis (from the low potassium), as well as profound systemic manifestations. Out of all of the variants, this form is the most severe. |
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CID11:ID_1424120171
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dki-india-ID_1424120171
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Concluído
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13 August 2026
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