A rare case of 2q37 deletion syndrome presented with patent foramen ovale

Abstract

This case report presents a 3-year-old female child diagnosed with 2q37 deletion syndrome and patent foramen ovale, and the improvement in hypotonia and gross motor delay after 1 year of physical therapy. This case highlights the importance of thorough examination and diagnostic testing in identifying underlying causes of developmental delays.

Keywords: 2q37 deletion syndrome; cardiac anomalies; chromosome 2; comparative genomic hybridization; patent foramen ovale; single nucleotide polymorphism.