Yalcintepe, SinemZhuri, DrenusheSezginer Guler, HazalAtli, EnginDemir, SelmaAtli, Emine IkbalMail, Cisem2024-06-122024-06-1220221661-87691661-8777https://doi.org/10.1159/000519149https://hdl.handle.net/20.500.14551/21988Jacobsen syndrome is a rare congenital disorder that is caused by the deletion of several genes in chromosome 11. A 10-year-old female with congenital heart disease, dextrocardia, and coarse facial appearance was examined in our medical genetics clinic. Chromosome analysis and array-CGH showed a copy number loss of 9 Mb in the 11q24.2q25 region. Herein, we report her clinical findings. This is the first case of Jacobsen syndrome with dextrocardia.en10.1159/000519149info:eu-repo/semantics/openAccessJacobsen SyndromeDextrocardiaArray-CGHCongenital Heart DiseaseDeletion 11qInterstitial 11q24 DeletionParis-Trousseau-SyndromePlateletsDefectChildGeneArticle133235239Q4WOS:0007506165000012-s2.0-8512452859035707598Q4