Cleidocranial dysplasia with hypermobile Ehlers-Danlos syndrome: A case report

Cleidocranial dysplasia (CCD) is a rare genetic skeletal syndrome. The most common features are open fontanelles, hypertelorism, mid-face retrusion, hypoplasia, or aplasia of the clavicles leading to excessive shoulder mobility, dental abnormalities such as supernumerary, and impacted teeth. This ca...

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Detalles Bibliográficos
Autores principales: Ibrahim, Rengin, Hamadah, Omar, Abdul-Hak, Mahmoud, Alshawa, Aladdin, Alouda, Mohamad Alhasan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649364/
https://www.ncbi.nlm.nih.gov/pubmed/36388612
http://dx.doi.org/10.1016/j.radcr.2022.10.038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649364/
https://www.ncbi.nlm.nih.gov/pubmed/36388612
http://dx.doi.org/10.1016/j.radcr.2022.10.038

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