Infant and adolescent with DiGeorge syndrome

(A) Infant with DiGeorge syndrome has the typical hypertelorism, downward-slanting 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.