Glaudemans type isolated autosomal dominant hypomagnesaemia (Q99739): Difference between revisions

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Latest revision as of 16:24, 16 August 2026

Isolated autosomal dominant hypomagnesemia, Glaudemans type is a form of familial primary hypomagnesemia, characterised by low serum magnesium values but normal urinary magnesium values. The typical clinical features are recurrent muscle cramps, tetanic episodes, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal.

Language	Label	Description	Also known as
default for all languages	ID_1038958214
English	Glaudemans type isolated autosomal dominant hypomagnesaemia	Isolated autosomal dominant hypomagnesemia, Glaudemans type is a form of familial primary hypomagnesemia, characterised by low serum magnesium values but normal urinary magnesium values. The typical clinical features are recurrent muscle cramps, tetanic episodes, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal.