2024/12/31 by Khalsi, F., Belhadj I, BenRomdhane M +6
#Caylercardiofacial syndrome #Fluorescent in situ hbridization #Hybridation fluores- cente in situ #Syndrome cardio-facial de Cayler #asymétrie faciale #cardiopathies congénitales #congenital heart defects #facial assymetry
paper · doi:10.71566/pist-rmp-194748
Facial asymmetries to the tears are rare. We report a pediatric original case that may fall within the framework of a Cayler syndrome. Through its clinical presentation, we will discuss differential diagnoses, associatedforms,itsetiology,anditsmanagement. Atthepediatricward,inafemaleinfant,duringhospi- talizationforbronchiolitis,wasdiscoveredalackofmobilityofthelabialcommissureontherightside,only when crying. The rest of the examination was unremarkable, except ipsilateral microtia. Genetically,karyotypewas46,XY,22q11withoutmicrodeletion. Theechocardiogramshowedpulmonary stenosis. Asymmetrywithtears has been described inthe literature,through associationwith microdeletion 22q11syndrome. Itisimportanttoknowthispathologyinordertosearchassociatedabnormalities(FISH 22q11,cardiacDopplerultrasound)butalsotoeducate,toreassurefamiliesoftenworriedbythesituation.