Autosomal dominant primary hypomagnesemia with hypocalciuria
What is Autosomal dominant primary hypomagnesemia with hypocalciuria?
A mild form of familial primary hypomagnesemia (FPH), characterized by extreme weakness, tetany and convulsions. Secondary disturbances in calcium excretion are observed.
Other condition names
- HOMG2
- Isolated autosomal dominant hypomagnesemia
- Isolated renal magnesium wasting
- Renal hypomagnesemia type 2
Inheritance type
Autosomal dominant
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- All ages
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.