Ellis van Creveld syndome

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Abstract

Ellis-van Creveld syndrome (EVC) or chondroectodermal dysplasia is a rare autosomal recessive disorder. It is a tetrad of chondrodysplasia, ectodermal dysplasia, polydactyly, and congenital heart disease. In several case reports, dysplasia involving other organs has also been identified. The exact prevalence is unknown, but the syndrome seems more common among the Amish community. Many Indian cases have also been reported. This report describes a classical case of EVC syndrome in a 22 year old woman of Indian origin born of a consanginous marriage. The patient had chondrodysplasia of tubular bones resulting in disproportionate dwarfism, postaxial polydactyly, severely dystrophic nails, partially absent teeth, pectus excavatum with narrow chest, knock knees and AV canal defect. © JAPI.

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APA

Ghanekar, J., Sangrampurkar, S., Hulinaykar, R., & Ahmer, T. (2009). Ellis van Creveld syndome. Journal of Association of Physicians of India, 57(7), 532–534. https://doi.org/10.1007/978-1-60327-161-5_63

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