CAPDEPON SYNDROME

Abstract

Capdepon syndrome, also known as Stenton–Capdepon syndrome, is a hereditary disease that affects the normal development of teeth, particularly disrupting the formation of enamel and dentin. In this syndrome, changes in tooth color, thinning and rapid wear of enamel, as well as the appearance of short teeth may be observed. It is also referred to as “decorative root teeth” or “mesoectodermal odontopathy.” This article provides a scientific analysis of the pathogenetic mechanisms, clinical manifestations, diagnostic criteria, and preventive measures of Capdepon syndrome. The results of the study highlight the significant scientific and practical importance of early detection and effective control of Capdepon syndrome in promoting a healthy lifestyle among the population..