Isolated autosomal dominant hypomagnesemia, Glaudemans type

Orpha code: 199326OMIM code:

Definition

Isolated autosomal dominant hypomagnesemia, Glaudemans type (IADHG) is a form of familial primary hypomagnesemia (FPH, see this term), 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.

Disease data
Classification

Disease

ORPHA code
199326
OMIM code
-
ICD10 code
E83.4
ICD11 code
5C64.41

No additional description.

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