Bartter syndrome with hypocalcaemia (Q85250): 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 na presença de níveis baixos de cálcio sérico no sangue (hipocalcemia), especificamente menos de 2,1 mmol/L ou 9 mg/dl ou um nível de cálcio ionizado inferior a 1,1 mmol/L ou 4,5 mg/dL.
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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.

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.
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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.

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