Crouzon disease is a genetic syndrome characterized by premature obliteration and ossification of two or more sutures of the skull [most often the saggital and coronal sutures], exophthalmoses and mid-facial hypoplasia, resulting in a craniofacial dysostosis. It is often called a craniostenosis. (Mary, Kugler) The type of stenosis is determined by the sutures which are obliterated. Types include scaphocephaly in which the head looks like a boat, oxycephaly in which the top of the head is pointed, wedge-shaped skull and oblique types have been documented in literature. (Lukasz, Mutusiak) Crouzon's disease is a rare disease that affects 1 in 25000 live births worldwide ...
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