Caso clínico-radiológico para diagnóstico

Abstract

Cleidocranial dysostosis (CCD) is a rare inherited congenital disorder that presents an autosomal dominant pattern with variable expressivity. Clinically, it is characterized by agenesis or dysgenesis of clavicle, bell shaped thorax, large fontanelles, delayed or absent ossifcation of pubic bones and hypoplasia of iliac wings. Both infant and permanent teeth eruption is delayed. Shoulder dislocation and osteoarthritis are complications described in adults. There is no specifc treatment for this condition. Case report and literature reviews are presented.