Pfeiffer syndrome, a rare genetic disorder, is characterized by craniosynostosis and other birth defects. There are three subtypes of Pfeiffer syndrome. In type I Pfeiffer syndrome the individual usually has a normal lifespan and typical intelligence. Individuals with types II and II have more severe birth defects that can affect brain development and function. Signs and symptoms of Pfeiffer syndrome include a high forehead, prominent lower jaw, protrusion of the eyes, beaked nose, and short fingers and toes. There is no cure for Pfeiffer syndrome. Read more: Pfeiffer Syndrome Article
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