Antenatal Bartter syndrome (Q85249): Difference between revisions
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Este é um defeito hereditário raro caracterizado por poliidrâmnio (aumento de água no útero) devido à poliúria no útero. Em contraste com a Síndrome de Bartter Clássica e a Síndrome de Gitelman, a variante pré-natal da Síndrome de Bartter tem tanto as características de alcalose metabólica (pelo potássio baixo), quanto manifestações sistêmicas profundas. De todas as variantes, esta forma é a mais grave. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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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| Property / Canonical URI: https://id.who.int/icd/entity/1424120171 / rank | |||||||||||||||
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CID11:ID_1424120171 | |||||||||||||||
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dki-india-ID_1424120171 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1424120171 / rank | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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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 |
|---|---|---|---|
| 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. |
Statements
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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