نتایج جستجو برای: ellis van creveld syndrome

تعداد نتایج: 689663  

Journal: :Medicina oral, patologia oral y cirugia bucal 2009
Daniela Alves-Pereira Leonardo Berini-Aytés Cosme Gay-Escoda

Ellis-van Creveld syndrome is a genetic disorder that was first described by Richard Ellis and Simon van Creveld in 1940. The four principal characteristics are chondrodysplasia, polydactyly, ectodermal dysplasia and congenital heart defects. The orofacial manifestations include multiple gingivolabial musculofibrous fraenula, dental anomalies, hypodontia and malocclusion. The disease can be dia...

Journal: :Pediatric dentistry 2004
Abel Cahuana Camila Palma Wilber Gonzáles Esther Geán

Ellis-van Creveld syndrome, or chondroectodermal dysplasia, is an autosomal recessive disorder with characteristic clinical manifestations. Its incidence in the general population is low. The oral manifestations of Ellis-van Creveld are found in soft tissues and teeth, but the dental literature on the subject is scarce. In the last 20 years, 5 cases of Ellis-van Creveld syndrome have been follo...

1978
Subash Singh Vandana Arya M Jonathan Daniel Vijeev Vasudevan

Ellis-van Creveld syndrome also known as chondroectodermal dysplasia or mesoectodermal dysplasia; a rare genetic disorder of the skeletal dysplasia. 'Six-fingered dwarfism' (digital integer deficiency) was an alternative designation used for this condition when it was being studied in the Amish. It is characterized by short-limb dwarfism, polydactyly, malformation of the bones of the wrist, dys...

Journal: :Journal of the Royal Army Medical Corps 1988
J C Nainby-Luxmoore

The first reported case of Ellis--van Creveld syndrome in a Gurkha child is described, and the implications of the syndrome in this ethnic group are briefly considered.

Journal: :dental research journal 0
shaik sameeulla jayam raviraj suresh dirasantchu suman s. venkata

ellis–van creveld (evc) syndrome, a form of skeletal and chondroectodermal dysplasia, is an autosomal recessive disorder characterized by a tetrad of disproportionate dwarfism, postaxial polydactyly, ectodermal dysplasia, and heart defects. in the present article, we hereby present a case of a 13‑year‑old girl of indian ethnicity with evc syndrome with a remarkable number of classical oral and ...

معموری, غلامعلی, ناصری, فاطمه,

Ellis Van Creveld syndrome or chondroectodermal dysplasia is a rare disease characterized by the triad of postaxial polydactyly, chondrodisplasia of long bones , resulting in acromesomelic dwarfism, and ectodermal dysplasia. In this study , three newborns with this syndrome , consisting of    acromesomelic dwarfism , postaxial bilateral polydactyly , nail hypoplasia...

Journal: :Journal of Evolution of Medical and Dental Sciences 2014

تقی بغدادی, , نادر طوسی, ,

Ellis-van Creveld sydrome (Chondroectodermal dysplasia) is a hereditary form of short limb disproportionate dwarfism characterized by diffuse involvement of skeletal system and visceral organs. Two brothers affected by this syndrome are presented here following a brief account of the disease's manifestations.

Journal: :مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران 0
تقی بغدادی baghdadi t نادر طوسی toosi n

ellis-van creveld sydrome (chondroectodermal dysplasia) is a hereditary form of short limb disproportionate dwarfism characterized by diffuse involvement of skeletal system and visceral organs. two brothers affected by this syndrome are presented here following a brief account of the disease's manifestations.

2013
Rajashree Pradhan Sajeeb Mondal Shouvanik Adhya Sagar Dutta Richard W. B. Ellis

Ellis Van Creveld syndrome is a disease complex where all the three embryonic layers appear to be involved. This disorder is also called chondro ectodermal dysplasia or meso ectodermal dysplasia. It is a part of an emerging class of diseases called ciliopathies due to primary dysfunction of cilia. It is very rare; only about 150 cases have been described in the world literature and rarely been ...

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