Isolated autosomal dominant hypomagnesemia, Glaudemans type

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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://www.orphadata.org. Data version June 2024

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Isolated autosomal dominant hypomagnesemia, Glaudemans type?

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Advocacy Organizations

Mississippi Metabolics Foundation

Our mission at Mississippi Metabolics Foundation (MMF) is to advocate, educate, and support families in MS affected by genetic metabolic disorders/inborn errors of metabolism (IEM's). MMF promotes initiatives and further advancements in legislation, education, research, clinical trials, studies, therapies, targeted treatments, and eventual cures for IEM’s and all rare diseases.

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Clinical Trials

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