Familial Cleidocranial Dysplasia in a Neonate: A Case Report

• Main Authors: Kalyan Konda (Author), Devendar Katkuri (Author), Kasi Viswanath Reddy (Author), Joshua Rajan X (Author), Leslie Edward Lewis (Author)
• Formato: Livro
• Publicado em: Mashhad University of Medical Sciences, 2018-05-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence of 1 case per 1000,000 individuals. It is a form of predominantly autosomal dominant inheritance and is associated with a mutation in runt related transcription factor-2 gene mapped on chromosome 6p21...