Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy

Background KCNMA1 mutations have recently been associated with a wide range of dysmorphological, gastro-intestinal, cardiovascular, and neurological manifestations. Methods Whole exome sequencing was performed in order to identify the underlying pathogenic mutation in two cases presenting with diverse phenotypical manifestations that did not fit into well-known clinical entities. Results In an 8-year-old boy presenting with severe aortic dilatation, facial dysmorphism, and overgrowth at birth a de novo p.Gly375Arg KCNMA1 mutation was identified which has been reported previously in association with gingival hypertrophy, aortic dilatation, and developmental delay. Additionally, in a 30-week-old fetus with severe growth retardation and duodenal atresia a de novo p.Pro805Leu KCNMA1 mutation was identified. The latter has also been reported before in a boy with severe neurological manifestations, including speech delay, developmental delay, and cerebellar dysfunction. Conclusion The current report presents the first antenatal presentation of a pathogenic KCNMA1 mutation and confirms the specific association of the p.Gly375Arg variant with early onset aortic root dilatation, gingival hypertrophy, and neonatal overgrowth.

Automated summary

The study identifies pathogenic mutations in KCNMA1 gene associated with a wide range of clinical manifestations, including aortic dilatation, growth retardation, and neurological dysfunction. The p.Gly375Arg variant is linked to aortic root dilatation, gingival hypertrophy, and neonatal overgrowth, while the p.Pro805Leu variant is associated with severe neurological manifestations.