Isolated autosomal dominant hypomagnesemia, Glaudemans type

MONDO:0016048

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

1 clinical trial for this condition and its sub-types, 0 tagged with Isolated autosomal dominant hypomagnesemia, Glaudemans type itself.

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↑ Familial primary hypomagnesemia with normocalcuria (0)

Including sub-types (1) Tagged with Isolated autosomal dominant hypomagnesemia, Glaudemans type (0)

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