Familial hypokalaemia - hypomagnesaemia (Q99736): Difference between revisions
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A síndrome de Gitelman, que também é conhecida como hipocalemia-hipomagnesemia familiar, é uma doença tubular renal genética caracterizada por alcalose metabólica hipocalêmica em combinação com hipomagnesemia significativa e baixa excreção urinária de cálcio. | |||
| description / en | description / en | ||
Gitelman syndrome, also referred to as familial hypokalaemia-hypomagnesemia, is a genetic renal tubular disease characterised by hypokalaemia metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion. | |||
Revision as of 16:24, 16 August 2026
Gitelman syndrome, also referred to as familial hypokalaemia-hypomagnesemia, is a genetic renal tubular disease characterised by hypokalaemia metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1177986055 |
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| English | Familial hypokalaemia - hypomagnesaemia |
Gitelman syndrome, also referred to as familial hypokalaemia-hypomagnesemia, is a genetic renal tubular disease characterised by hypokalaemia metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion. |
