Familial primary hypomagnesemia with normocalcuria
MONDO:0017626Familial 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.
1 clinical trial for this condition and its sub-types.
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Familial primary hypomagnesemia with normocalciuria and normocalcemia
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Hypomagnesemia, seizures, and intellectual disability
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Hypomagnesemia, seizures, and intellectual disability 1
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Hypomagnesemia, seizures, and intellectual disability 2
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Intestinal hypomagnesemia 1
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Isolated autosomal dominant hypomagnesemia, Glaudemans type
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Renal hypomagnesemia 4
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Renal hypomagnesemia 6
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