Autosomal dominant primary hypomagnesemia with hypocalciuria
ORPHA:34528· ICD-10 E83.4
Definition
A mild form of familial primary hypomagnesemia (FPH), characterized by extreme weakness, tetany and convulsions. Secondary disturbances in calcium excretion are observed.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant
- Age of onset
- All ages