The objectives of this study were i) to conduct a comprehensive review of the literature on
hypo-hyperdontia, and ii) to categorize the reported cases based on occurrence. An …

M arfan syndrome is an autosomal dominant genetic disorder of connective tissue origin that
can affect multiple organs. Various oral manifestations have been associated with this …

Aim A systematic literature review on oral and craniofacial manifestations of Ellis-Van
Creveld syndrome was performed. Methods From 2 databases were selected 74 articles …

Ellis-van Creveld syndrome (EVC) or chondroectodermal dysplasia is an autosomal
recessive disorder, characterized by dwarfism, polydactyly, hypoplastic fingernails and …

Purpose The objective of this case series was to determine the oral, dental and craniofacial
features of patients with EvC syndrome. Material and methods Eight patients with EvC …

The aim of this systematic review was to describe the clinical and genetic features of
syndromes showing oligodontia as a sign. The review was performed according to the …

Ellis–van Creveld (EVC) syndrome, a form of skeletal and chondroectodermal dysplasia, is
an autosomal recessive disorder characterized by a tetrad of disproportionate dwarfism …

Ellis van Creveld syndrome (EVC) is a rare autosomal recessive disorder also called
chondroectodermal dysplasia. This study reports on a 40‐year‐old woman from Iran with a …

Abstract Introduction Ellis‐van Creveld (EVC) syndrome is an autosomal recessive disorder
predominantly characterized by a disproportionate dwarfism, ectodermal dysplasia …

This paper presents a case study of a young adult from the late Neolithic Yangshao cultural
period site (∼ 3300–2900 years BC) of Guanjia (关家) located in Henan Province on the …