Cleidocranial dysplasia: A rare case report

• Asıl Yazarlar: Akshay A Dhobley (Yazar), Aparna V Thombre (Yazar), Dipak Ghatage (Yazar), Ranu Ingole Patil (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Wolters Kluwer Medknow Publications, 2023-01-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

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...