Primary hypomagnesemia with secondary hypocalcemia
Synonyms: HOMG1 | HSH | Hypomagnesemia caused by selective magnesium malabsorption | Hypomagnesemia intestinal type 1 | Intestinal hypomagnesemia with secondary hypocalcemia | PHSH
Primary hypomagnesemia with secondary hypocalcemia (PHSH) is a form of familial primary hypomagnesemia (FPH see this term) characterized by severe hypomagnesemia and secondary hypocalcemia associated with neurological symptoms including generalized seizures tetany and muscle spasms. PHSH may be fatal or may result in chronic irreversible neurological complications.
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 October 2023.
Newly diagnosed with
Primary hypomagnesemia with secondary hypocalcemia?
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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).
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.
Clinical Trials
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