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Chondro-Ectodermal Dysplasia (Ellis-van Creveld Syndrome) Report of a Case and Review of the Literature
Narciso A. Ferrero; Osvaldo O. Pozo; Emilio S. Morresi
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Department of Pediatrics "Casa Cuna", Buenos Aires University, School of Medicine and the Department of Radiology and Pediatrics, Ezeiza Policlinic, Buenos Aires
1961 by The Journal of Bone and Joint Surgery, Incorporated
The Journal of Bone & Joint Surgery.  1961; 43:1230-1236 
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Abstract

A case of Ellis-van Creveld syndrome (chondro-ectodermal dysplasia) is reported in a boy, nine years and nine months old. The main findings were polydactyly (both hands), ectodermal dysplasia (teeth and nails), and typical chondrodystrophial lesions. Congenital cardiac anomalies were absent. All studies, including the hemogram, blood chemistry, electrocardiogram, electroencephalogram, and psychometric and ophthalmoscopic examinations were normal. There was no consanguinity or genetic antecedents of the process in the parents. One brother and two half brothers were normal. From a review of the literature, this would appear to be the twenty-ninth case and the first reported from South America.

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    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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