Bartter syndrome with hypocalcaemia (Q85250): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_1757681822 | |||
| Property / CURIE: CID11:ID_1757681822 / rank | |||
Normal rank | |||
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 in the presence of low serum calcium levels in the blood (hypocalcaemia), specifically less than 2.1 mmol/L or 9 mg/dl or an ionized calcium level of less than 1.1 mmol/L or 4.5 mg/dL.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1757681822 |
||
| English | Bartter syndrome with hypocalcaemia |
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 in the presence of low serum calcium levels in the blood (hypocalcaemia), specifically less than 2.1 mmol/L or 9 mg/dl or an ionized calcium level of less than 1.1 mmol/L or 4.5 mg/dL. |
Statements
CID11:ID_1757681822
0 references
