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Familial primary hypomagnesemia with normocalcuria

Familial primary hypomagnesemia with normocalcuria (FPHN) is a form of familial primary hypomagnesemia (FPH) which is characterized by low magnesium values but normal calcium values in the serum. The disorder consists of three distinct forms which are: autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia (ARPHN), familial primary hypomagnesemia with normocalcuria and normocalcemia (FPHNN) and isolated autosomal dominant hypomagnesemia, Glaudemans type.

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Familial primary hypomagnesemia with normocalciuria and normocalcemia 0 trials Sub-types →
Intestinal hypomagnesemia 1 0 trials
Isolated autosomal dominant hypomagnesemia, Glaudemans type 0 trials