renal hypomagnesemia 6

A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gen

A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24.

Signs and symptoms

• Impaired renal tubular reabsorption of magnesium
• Hypomagnesemia
• Vertigo
• Muscle weakness
• Headache

Also known as: HOMG6