Infant and adolescent with DiGeorge syndrome

(A) Infant with DiGeorge syndrome has the typical hypertelorism, antimongoloid slant of the eyes, ear malformation, and peculiar mouth.
(B) Older child with DiGeorge syndrome depicts characteristic facial features, which become more subtle with age. Relatively consistent features are hooded eyelids, a bulbous nose tip, a broad nasal bridge, posteriorly rotated ears, simple ear helices, and micrognathia. This child has posteriorly rotated ears with simple helices, slightly hooded eyelids, and a slightly bulbous nose tip.