Hypomagnesemia primary
A progressive renal disorder characterized by excessive urinary Ca(2+) and Mg(2+) excretion. There is progressive loss of kidney function, and in about 50% of cases, the need for renal replacement therapy by the second decade of life. Germline mutations in the CLDN16 gene have been identified. OMIM: 603959
Also Known As:
Hypomagnesemia 3, Renal; Hypomagnesemia, Primary, Due To Defect In Renal Tubular Transport Of Magnesium; Hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis; Hypomagnesemia, isolated renal; Magnesium, defect in renal tubular transport of
Networked: 0
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results