ea0099ep1307 | Late Breaking | ECE2024
Cheikh Mariem
, Zakaria Cheibete
, Mokhtar Mohamed
, Rifai Kaoutar
, Hinde Iraqi
, Elhassan Gharbi Mohamed
Introduction: DiGeorge syndrome is a genetic abnormality caused by a microdeletion of chromosome 22. Chromosome 22q1 1.2 microdeletion was first identified in 1992 as the common genetic anomaly associated with a range of conditions previously known as DiGeorge or velocardiofacial syndrome.Case report: A 17-year-old Moroccan male was mildly mentally challenged and had seizures from the age of 9 years. He had dysmorphic facial features, and mild tortuosity...