Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature

Palumbo et al. (2015) reported a female with chromosome 12q24.31 microdeletion presenting with neurodevelopmental delay, seizures, intellectual disability, and dysmorphic features, who was also noted to have a patent foramen ovale requiring interatrial repair at 18 months of age. Although they did c