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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

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