Apert syndrome

Alternative names:

acrocephalosyndactyly type 1

Treatment:

Treatment consists of surgery to correct the skull, mid-face, palate, after evaluation by a multispecialty cranio-facial team at a children's medical center.

Expectations (prognosis):

The prognosis varies from child to child.

Complications:

Other congenital abnormalities may exist and should be evaluated on an individual basis.