Also Known As
CLDN16 familial primary hypomagnesemiaCLDN16 primary hypomagnesemiaFHHNC without severe ocular involvementHOMG3familial primary hypomagnesemia caused by mutation in CLDN16familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvementisolated renal hypomagnesemiaprimary hypomagnesemia caused by mutation in CLDN16primary hypomagnesemia due to defect in renal tubular transport of magnesiumrenal hypomagnesemia type 3hypercalciuria, childhood, self-limitinghypomagnesemia 3, renalhypomagnesemia, familial, with hypercalciuria and nephrocalcinosishypomagnesemia, familial, with hypercalciuria and nephrocalcinosis hypercalciuria, childhood, self-limiting, includedhypomagnesemia, isolated renalhypomagnesemia, primary, due to defect in renal tubular Transport Of magnesiumhypomagnesemia, primary, due to defect in renal tubular Transport of magnesiummagnesium, defect in renal tubular transport of
Definition
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia (FPH), characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure.