Hypomagnesaemia due to selective magnesium malabsorption (Q99745): Difference between revisions
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A hipomagnesemia causada por má absorção seletiva de magnésio ou tetania hipomagnesêmica é uma forma de hipomagnesemia primária familiar caracterizada por níveis séricos de magnésio muito baixos e excreção renal normal de magnésio, associada à hipocalcemia. Os pacientes geralmente apresentam-se no período neonatal e sofrem de inquietação, tremor, tetania e convulsões. É uma doença grave que, se não tratada, é fatal. | |||
| description / en | description / en | ||
Hypomagnesaemia caused by selective magnesium malabsorption or hypomagnesaemic tetany is a form of familial primary hypomagnesaemia characterised by very low serum magnesium (Mg2+) levels and normal renal Mg2+ excretion, associated with hypocalcaemia. Patients usually present in the neonatal period and suffer from restlessness, tremor, tetany and overt seizures. It is a severe disorder, which, if left untreated, is fatal. | |||
Revision as of 16:25, 16 August 2026
Hypomagnesaemia caused by selective magnesium malabsorption or hypomagnesaemic tetany is a form of familial primary hypomagnesaemia characterised by very low serum magnesium (Mg2+) levels and normal renal Mg2+ excretion, associated with hypocalcaemia. Patients usually present in the neonatal period and suffer from restlessness, tremor, tetany and overt seizures. It is a severe disorder, which, if left untreated, is fatal.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1707590653 |
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| English | Hypomagnesaemia due to selective magnesium malabsorption |
Hypomagnesaemia caused by selective magnesium malabsorption or hypomagnesaemic tetany is a form of familial primary hypomagnesaemia characterised by very low serum magnesium (Mg2+) levels and normal renal Mg2+ excretion, associated with hypocalcaemia. Patients usually present in the neonatal period and suffer from restlessness, tremor, tetany and overt seizures. It is a severe disorder, which, if left untreated, is fatal. |
