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Cleidocranial dysostosis: a case report with clinical illustration

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 patien...

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Autores principales: Villamil, Vanesa, Pruneda, Ramón Ruiz, Ibieta, María Fernández, Cánovas, César Salcedo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308938/
https://www.ncbi.nlm.nih.gov/pubmed/34367447
http://dx.doi.org/10.11604/pamj.2021.38.368.29204
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author Villamil, Vanesa
Pruneda, Ramón Ruiz
Ibieta, María Fernández
Cánovas, César Salcedo
author_facet Villamil, Vanesa
Pruneda, Ramón Ruiz
Ibieta, María Fernández
Cánovas, César Salcedo
author_sort Villamil, Vanesa
collection PubMed
description 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.
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spelling pubmed-83089382021-08-06 Cleidocranial dysostosis: a case report with clinical illustration Villamil, Vanesa Pruneda, Ramón Ruiz Ibieta, María Fernández Cánovas, César Salcedo Pan Afr Med J Case Report 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. The African Field Epidemiology Network 2021-04-15 /pmc/articles/PMC8308938/ /pubmed/34367447 http://dx.doi.org/10.11604/pamj.2021.38.368.29204 Text en Copyright: Vanesa Villamil et al. https://creativecommons.org/licenses/by/4.0/The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Villamil, Vanesa
Pruneda, Ramón Ruiz
Ibieta, María Fernández
Cánovas, César Salcedo
Cleidocranial dysostosis: a case report with clinical illustration
title Cleidocranial dysostosis: a case report with clinical illustration
title_full Cleidocranial dysostosis: a case report with clinical illustration
title_fullStr Cleidocranial dysostosis: a case report with clinical illustration
title_full_unstemmed Cleidocranial dysostosis: a case report with clinical illustration
title_short Cleidocranial dysostosis: a case report with clinical illustration
title_sort cleidocranial dysostosis: a case report with clinical illustration
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308938/
https://www.ncbi.nlm.nih.gov/pubmed/34367447
http://dx.doi.org/10.11604/pamj.2021.38.368.29204
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