Digeorge syndrome facial features

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The 22q In children with this syndrome, a tiny piece of chromosome 22 is missing. This can cause many health problems. These problems may range from heart defects and developmental delays to seizures.
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What's to know about DiGeorge syndrome?

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DiGeorge syndrome: Causes, symptoms, and treatment

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Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome)

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Deletion 22q Characteristic facial features include angular facies; small, posteriorly rotated ears with abnormal pinnae; and palatal abnormalities, such as a cleft of palate and submucosal cleft palate Figure 1, Figure 2, Figure 3, Figure 4. Velopharyngeal incompetence may be the only clinical presentation. Learning difficulties occur in more than 90 percent of affected individuals.
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