Familial primary hypomagnesemia with normocalciuria and normocalcemia

MONDO:0018101

Familial primary hypomagnesemia with normocalciuria and normocalcemia (FPHNN) is a form of familial primary hypomagnesemia (FPH), characterized by low serum magnesium (Mg) values but inappropriate normal urinary Mg values (i.e. renal hypomagnesemia). The typical symptoms are weakness of the limbs, vertigo, headaches, seizures, brisk tendon reflexes and mild to moderate psychomotor delay.

1 clinical trial for this condition and its sub-types, 0 tagged with Familial primary hypomagnesemia with normocalciuria and normocalcemia itself.

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Sub-types of Familial primary hypomagnesemia with normocalciuria and normocalcemia

Hypomagnesemia, seizures, and intellectual disability 0 trials
2 sub-types
- Hypomagnesemia, seizures, and intellectual disability 1 0 trials
- Hypomagnesemia, seizures, and intellectual disability 2 0 trials
Renal hypomagnesemia 4 0 trials
Renal hypomagnesemia 6 0 trials

Including sub-types (1) Tagged with Familial primary hypomagnesemia with normocalciuria and normocalcemia (0)

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