Cleidocranial Dysplasia with Autosomal Dominant Inheritance Pattern

Cleidocranial dysplasia (CCD) is an autosomal dominant disease with a wide range of expression, characterized by clavicular hypoplasia, retarded cranial ossification, delayed bone and teeth development, supernumerary teeth, stomatognathic, craniofacial and skeletal abnormalities. This paper presents...

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Detalles Bibliográficos
Autores principales: Bhargava, P, Khan, S, Sharma, R, Bhargava, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145514/
https://www.ncbi.nlm.nih.gov/pubmed/25184084
http://dx.doi.org/10.4103/2141-9248.138042

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145514/
https://www.ncbi.nlm.nih.gov/pubmed/25184084
http://dx.doi.org/10.4103/2141-9248.138042

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