renal hypomagnesemia 2

info · Genetic · ICD-10: E83.4

A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.

Signs and symptoms

Renal magnesium wasting
Hypomagnesemia
Generalized muscle weakness
Seizure
Chondrocalcinosis
Hypocalciuria
Hypokalemia
Renal insufficiency

Also known as: HOMG2; autosomal dominant primary hypomagnesemia with hypocalciuria