Ellis–Van Creveld syndrome in siblings: A rare case report | Zendy

Sabitha Gokulraj | Zendy; N Mohan | Zendy; JBabususai Raj | Zendy; SYasmeen Ahamed | Zendy; CJ Stephen Arokiaraj | Zendy; ACicilia Subbulakshmi | Zendy

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

Author(s) -

Sabitha Gokulraj,

N Mohan,

JBabususai Raj,

SYasmeen Ahamed,

CJ Stephen Arokiaraj,

ACicilia Subbulakshmi

Publication year - 2016

Publication title -

journal of pharmacy and bioallied sciences

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.268

H-Index - 36

eISSN - 0976-4879

pISSN - 0975-7406

DOI - 10.4103/0975-7406.191954

Subject(s) - polydactyly , medicine , ectodermal dysplasia , dysplasia , dermatology , pediatrics , pathology , anatomy

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.

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