What is another word for Pfeiffer Syndrome?
Pronunciation: [fˈe͡ɪfə sˈɪndɹə͡ʊm] (IPA) 
Pfeiffer Syndrome is a rare genetic condition that affects the bones of the skull, face, and hands. It is primarily defined by premature fusion of the skull bones, called craniosynostosis, leading to abnormal development of the face and head. While there are no direct synonyms for Pfeiffer Syndrome, it is a type of craniosynostosis, which refers to any premature fusion of the skull bones. Other synonyms may include acrocephalosyndactyly, which is a group of conditions that affect both the skull and hands, and Apert Syndrome, which is another type of craniosynostosis that affects the shape of the skull and face.
