Literature DB >> 8155349

[The Ellis-Van Creveld syndrome. Apropos 2 clinical cases].

J M Santos1, J Pipa, L Antunes, O Neves, C Nascimento, C Cabral, A Costa, O Barros, J Carvalho, F Angelo.   

Abstract

The chondroectodermal dysplasia--Ellis-Van Creveld Syndrome--is an unusual form of congenital disease, genetically transmitted with a recessive autosomal pattern, which involves the skeletal system, nails and teeth. In about 50 to 60 percent of cases, the affected individuals show cardiac abnormalities, and the most common are single atrium, large atrial septal defect, ostium primum type. Other abnormalities may accompany these lesions, such as aortic atresia, hypoplasia of the ascending aorta or of the left ventricle. About half of the patients die in the childhood due to cardiorespiratory complications. Two cases are described with this syndrome, a male and a female, with 54 and 45 years old respectively; they were followed in our Departments and showed congestive heart failure and single atrium. These cases led us to review the subject; we believe that the unusual longevity of these patients can be related to their relatively benign cardiac disease.

Entities:  

Mesh:

Year:  1994        PMID: 8155349

Source DB:  PubMed          Journal:  Rev Port Cardiol        ISSN: 0870-2551            Impact factor:   1.374


  1 in total

1.  Corrected ASD: case closed?

Authors:  Luis V Paiva; Rui Providencia; Joaquim Sá; R Bastiaenen; Ana Botelho; Paula Mota; Antonio Leitao-Marques
Journal:  BMJ Case Rep       Date:  2011-08-04
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.