Catalog
Primary familial hypomagnesaemia
No MMS code
Link to WHO Definition
Primary familial hypomagnesaemia – http://id.who.int/icd/entity/1430309389
Familial primary hypomagnesemia is due to a defect of intestinal magnesium (Mg2+) absorption, or to a defective renal magnesium (Mg2+) reabsorption.
Parents
Children
- Glaudemans type isolated autosomal dominant hypomagnesaemia
- Familial hypokalaemia - hypomagnesaemia
- Hypomagnesaemia with hypocalciuria
- Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis - severe ocular involvement
- Hypomagnesaemia due to selective magnesium malabsorption
- Familial hypokalaemia - hypercalciuria
- Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis
- Hypomagnesaemia with normocalciuria