Ellis-Van Creveld syndrome in siblings: A rare case report

Ellis-Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis-Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dys...

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Bibliographic Details
Published in:Journal of pharmacy & bioallied science 2016-10, Vol.8 (5), p.179-181
Main Authors: Gokulraj, Sabitha, Mohan, N, Raj, J, Ahamed, S, Stephen Arokiaraj, C, Subbulakshmi, A
Format: Article
Language:English
Subjects:
Care and treatment
Case Report
Chondroectodermal dysplasia
Congenital heart disease
Ellis-Van Creveld syndrome
Genetic aspects
Risk factors
siblings
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Summary:Ellis-Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis-Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dysplasia, and cardiac defects. Here, we are presenting a very rare case of Ellis-Van Creveld syndrome in siblings.
ISSN:0975-7406
0976-4879
0975-7406
DOI:10.4103/0975-7406.191954