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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.

35 clinical trials for this condition and its sub-types.

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Sub-types

Hypomagnesemia, seizures, and intellectual disability (0) Hypomagnesemia, seizures, and intellectual disability 1 (0) Hypomagnesemia, seizures, and intellectual disability 2 (0) Renal hypomagnesemia 4 (0) Renal hypomagnesemia 6 (0)

Broader categories

Disease (618) Metabolic disease (215) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Inborn errors of metabolism (42) Human disease (14) Familial primary hypomagnesemia (4) Disease of genetic or genomic mechanism (2) Inborn metal metabolism disorder (1)
Trials to join now! 18 Not yet recruiting 5 Not yet finished but already full! 6 Completed 6
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