Cleidocranial Dysplasia: A Rare Case Report

Cleidocranial dysplasia (CCD) is a rare hereditary disease of unknown etiology which was previously known as cleidocranial dysostosis. It usually follows an autosomal dominant mode of transmission with no predilection of genre or ethnic group. It is caused by a mutation of RUNX2, characterized by ge...

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Detalles Bibliográficos
Autores principales: Dhobley, Akshay A., Thombre, Aparna V., Ghatage, Dipak, Patil, Ranu Ingole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485440/
https://www.ncbi.nlm.nih.gov/pubmed/37693969
http://dx.doi.org/10.4103/jpbs.jpbs_212_23

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485440/
https://www.ncbi.nlm.nih.gov/pubmed/37693969
http://dx.doi.org/10.4103/jpbs.jpbs_212_23

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