Classic Bartter syndrome (Q85244): Difference between revisions
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Este é um defeito hereditário raro no ramo ascendente espesso da alça de Henle. É caracterizada por baixos níveis de potássio (hipocalemia), aumento do pH sanguíneo (alcalose) e pressão arterial normal a baixa. Existem dois tipos de síndrome de Bartter: neonatal e clássica. Uma doença intimamente associada, a síndrome de Gitelman, é mais branda do que os dois subtipos da síndrome de Bartter. | |||
| description / en | description / en | ||
This is a rare inherited defect in the thick ascending limb of the loop of Henle. It is characterised by low potassium levels (hypokalaemia), increased blood pH (alkalosis), and normal to low blood pressure. There are two types of Bartter syndrome: neonatal and classic. A closely associated disorder, Gitelman syndrome, is milder than both subtypes of Bartter syndrome. | |||
Revision as of 10:36, 15 August 2026
This is a rare inherited defect in the thick ascending limb of the loop of Henle. It is characterised by low potassium levels (hypokalaemia), increased blood pH (alkalosis), and normal to low blood pressure. There are two types of Bartter syndrome: neonatal and classic. A closely associated disorder, Gitelman syndrome, is milder than both subtypes of Bartter syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1489214231 |
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| English | Classic Bartter syndrome |
This is a rare inherited defect in the thick ascending limb of the loop of Henle. It is characterised by low potassium levels (hypokalaemia), increased blood pH (alkalosis), and normal to low blood pressure. There are two types of Bartter syndrome: neonatal and classic. A closely associated disorder, Gitelman syndrome, is milder than both subtypes of Bartter syndrome. |
