Ellis Van Creveld Syndrome: A Case Report

Kumar, Sarath and Padmavathi, S. and Anuradha, G. and Kannan, A. and Krithika, C. L. (2021) Ellis Van Creveld Syndrome: A Case Report. Journal of Pharmaceutical Research International, 33 (61B). pp. 246-250. ISSN 2456-9119

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Official URL: https://doi.org/10.9734/jpri/2021/v33i61B35526

Abstract

Ellis Van Creveld Syndrome (EVC) is a infrequent inborn genetic disorder with an x-linked recessive pattern of inheritance. This is recognized by bilateral accessory little finger in upper extremity, short limbs, ectodermal dysplasia affecting teeth and nails, and congenital cardiac defect. The overall prevalence of this disease is 7 in 1000000. In this current case, a 9year old female patient reported with typical general and oral manifestations, which were key diagnostic features of EVC syndrome.

Item Type:	Article
Subjects:	Pacific Library > Medical Science
Depositing User:	Unnamed user with email support@pacificlibrary.org
Date Deposited:	28 Jan 2023 07:29
Last Modified:	30 Jul 2024 14:21
URI:	http://editor.classicopenlibrary.com/id/eprint/487

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