Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability?

aDepartment of Pediatric Genetics, Faculty of Medicine, Necmettin Erbakan University

bDepartment of Medical Genetics, Konya City Hospital

cDepartment of Pediatric Hematology, Konya City Hospital

dDepartment of Pediatric Hematology, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey

Received 2 June 2023 Accepted 26 March 2024.

Correspondence to Fayize Maden Bedel, MD, Department of Pediatric Genetics, Faculty of Medicine, Necmettin Erbakan University, Konya 42090, Turkey Tel: +90 5426013010; e-mail: [email protected]

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