Abstract
Cri-du-chat syndrome (SCDC) (OMIM # 123450) is a rare genetic disease in which there is a deletion of a part of the short arm of chromosome 5. It is estimated that this syndrome affects from 1 / 15,000 to 1 /50,000 children born in the world. One of the main characteristic is that all births present microcephaly. Another is a large incidence, double the population cardiac problems. The ob…