Syndromic Congenital Heart Disease in a Child with 6q24.3-q25.1 Microdeletion: A Case Report with Genotype–Phenotype Correlation
Chromosome 6q24.3-q25.1 microdeletion syndrome is a rare contiguous gene deletion disorder associated with multilevel congenital heart defects, growth abnormalities, and dysmorphic features. We report the case of an 8-month-old female child who presented with fever, cough, and respiratory distress. She had a history of...