Crouzon syndrome is an autosomal dominant disorder with variable expressivity, characterized by skull and facial malformations. Such alterations vary from case to case. Management requires multidisciplinary approach. Two cases of two sisters affected by Crouzon syndrome are described. Treatment was performed by orthopedic and orthodontic devices without surgery. Good esthetics and functional results were obtained. Five-year follow-up records are presented.
|Number of pages||9|
|Journal||Stomatologija / issued by public institution "Odontologijos studija" ... [et al.]|
|Publication status||Published - 2014|
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