Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family

• Những tác giả chính: A. Impellizzeri (Tác giả), G. Midulla (Tác giả), U. Romeo (Tác giả), C. La Monaca (Tác giả), E. Barbato (Tác giả), G. Galluccio (Tác giả)
• Định dạng: Sách
• Được phát hành: Hindawi Limited, 2018-01-01T00:00:00Z.
• Những chủ đề: article
• Truy cập trực tuyến: Connect to this object online.

Introduction. Cleidocranial dysplasia (CCD) is an inherited disease caused by mutations in the RUNX2 gene on chromosome 6p21. This pathology, autosomal dominant or caused by a spontaneous genetic mutation, is present in one in one million individuals, with complete penetrance and widely variable exp...