Catalog

Glaudemans type isolated autosomal dominant hypomagnesaemia

No MMS code

Link to WHO Definition

Glaudemans type isolated autosomal dominant hypomagnesaemia – http://id.who.int/icd/entity/1038958214

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.