Disorders

Primary Hypomagnesemia

Synonym(s): Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis, Isolated Renal Hypomagnesemia

Gene	Locus	Protein
CLDN16	3q28	Claudin-16

Laboratory	Test Method	Prenatal	Carrier *
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.