Autosomal dominant primary hypomagnesemia with hypocalciuria

Get in touch with RARE Concierge.

Contact RARE Concierge

Synonyms: HOMG2 | Isolated autosomal dominant hypomagnesemia | Isolated renal magnesium wasting | Renal hypomagnesemia type 2

A mild form of familial primary hypomagnesemia (FPH) characterized by extreme weakness tetany and convulsions. Secondary disturbances in calcium excretion are observed.

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 Data version July 2024

Newly diagnosed with
Autosomal dominant primary hypomagnesemia with hypocalciuria?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Clinical Trials

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