Pfeiffer syndrome Type 3: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include craniofacial abnormalities, cardiovascular malformations and early death is common. More detailed information about the symptoms, causes, and treatments of Pfeiffer syndrome Type 3 is available below.
See full list of 41 symptoms of Pfeiffer syndrome Type 3
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