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Up to: Renal tubular transport disease · Nephrocalcinosis · Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis

Renal hypomagnesemia 3

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.

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This condition has no sub-types.