{Reference Type}: Journal Article
{Title}: Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delay.
{Author}: Bosman W;Butler KM;Chang CA;Ganapathi M;Guzman E;Latta F;Chung WK;Claverie-Martin F;Davis JM;Hoenderop JGJ;de Baaij JHF;
{Journal}: Clin Kidney J
{Volume}: 17
{Issue}: 8
{Year}: 2024 Aug
{Factor}: 5.86
{DOI}: 10.1093/ckj/sfae211
{Abstract}: <B>UNASSIGNED: </B>Heterozygous variants in Transient receptor potential melastatin type 7 (TRPM7), encoding an essential and ubiquitously expressed cation channel, may cause hypomagnesemia, but current evidence is insufficient to draw definite conclusions and it is unclear whether any other phenotypes can occur.<BR><B>UNASSIGNED: </B>Individuals with unexplained hypomagnesemia underwent whole-exome sequencing which identified TRPM7 variants. Pathogenicity of the identified variants was assessed by combining phenotypic, functional and in silico analyses.<BR><B>UNASSIGNED: </B>We report three new heterozygous missense variants in TRPM7 (p.Met1000Thr, p.Gly1046Arg, p.Leu1081Arg) in individuals with hypomagnesemia. Strikingly, autism spectrum disorder and developmental delay, mainly affecting speech and motor skills, was observed in all three individuals, while two out of three also presented with seizures. The three variants are predicted to be severely damaging by in silico prediction tools and structural modeling. Furthermore, these variants result in a clear loss-of-function of TRPM7-mediated magnesium uptake in vitro, while not affecting TRPM7 expression or insertion into the plasma membrane.<BR><B>UNASSIGNED: </B>This study provides additional evidence for the association between heterozygous TRPM7 variants and hypomagnesemia and adds developmental delay to the phenotypic spectrum of TRPM7-related disorders. Considering that the TRPM7 gene is relatively tolerant to loss-of-function variants, future research should aim to unravel by what mechanisms specific heterozygous TRPM7 variants can cause disease.