RT Journal Article
T1 Cleidocranial dysostosis: a case report with clinical illustration.
A1 Villamil, Vanesa
A1 Pruneda, Ramón Ruiz
A1 Ibieta, María Fernández
A1 Cánovas, César Salcedo
K1 Cleidocranial dysostosis
K1 case report
K1 cleidocranial dysplasia
K1 supernumerary teeth
K1 wormian bones
AB Cleidocranial Dysostosis or Dysplasia (CCD) is an infrequent clinical condition, with an autosomal dominant hereditary mode of inheritance. Triad lesions: multiple supernumerary teeth, partial or complete absence of the clavicles and open sagittal sutures and fontanelles. Nine-year-old female patient comes to our service for outpatient consultation with the main complaint of upper limbs mobility restriction with shoulders hypermotility. The chest X-ray showed partial absence of the clavicles and a cone-shaped thorax. The diagnosis of CCD was performed. Treatment of these patients requires a multidisciplinary approach which includes orthopaedic and dental corrections. The premature diagnosis allows a proper orientation for the treatment, offering a better life quality for the patient.
YR 2021
FD 2021-04-15
LK http://hdl.handle.net/10668/18337
UL http://hdl.handle.net/10668/18337
LA en
DS RISalud
RD Apr 9, 2025