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Renal Hypomagnesemia 3
A hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that is caused by homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
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Overview
A hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that is caused by homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.