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.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.
Newly diagnosed with
Isolated autosomal dominant hypomagnesemia, Glaudemans type?
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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).
Louisiana Metabolic Disorders Coalition
We support, educate, and advocate for patients & families affected by metabolic disorders.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
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