Isolated autosomal dominant hypomagnesemia, Glaudemans type

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Isolated autosomal dominant hypomagnesemia, Glaudemans type

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: // Data version October 2023.

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Isolated autosomal dominant hypomagnesemia, Glaudemans type?

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Advocacy Organizations

Mississippi Metabolics Foundation

Mississippi Metabolics Foundation (MMF) was founded to raise awareness, educate, and provide support to those living or caring for someone with genetic metabolic disorders/inborn errors of metabolism (IEM).

Clinical Trials

For a list of clinical trials in this disease area, please click here.