Learning About Cri du Chat Syndrome. What is cri du chat syndrome? What are the symptoms of cri du chat syndrome? How is cri du chat syndrome diagnosed?
Cri-du-chat syndrome occurs in an estimated 1 in 20,000 to 50,000 newborns. This condition is found in people of all ethnic backgrounds.
Cri-du-chat syndrome is an autosomal deletion syndrome caused by a partial deletion of chromosome 5p and is characterized by a distinctive, high-pitched ...
Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p− (said minus) syndrome or Lejeune’s syndrome, is a rare genetic disorder due to a missing ...
The Cri du Chat syndrome (CdCS) is a genetic disease resulting from a deletion of variable size occurring on the short arm of chromosome 5 (5p-).
The geneticist Jerome Lejeune identified cri-du-chat syndrome in 1963. He also discovered the genetic abnormality that causes Down syndrome.
Cri du chat syndrome is rare. It is caused by a missing piece of chromosome 5. Most cases are believed to occur during the development of the egg or sperm.
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Cri du chat syndrome
What is Cri du Chat Syndrome? In 1963, a French geneticist, Jerome Lejeune, recognized several patients that had similar characteristics, one of which was a high ...
Cri du chat syndrome is a group of symptoms that result from missing a piece of chromosome number 5. The syndrome’s name is based on the infant’s cry, which is ...