Cri Du Chat Sindromul
Common symptoms include a distinctive cry that resembles the mewing of a.
Cri du chat sindromul. Its name is a french term referring to the characteristic cat like cry of affected children. Cri du chat syndrome cdcs or 5p is a rare genetic disorder in which a variable portion of the short arm of chromosome 5 is missing or deleted monosomic. Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. However they can become unbalanced as they are passed to the next generation.
Can you prevent cri du. About 10 percent of people with cri du chat syndrome inherit the chromosome abnormality from an unaffected parent. In general the severity of the symptoms is determined by the size and location of the deletion on chromosome 5. Cri du chat syndrome is due to a missing piece deletion of a specific part of chromosome 5 known as the p arm.
The condition affects an estimated 1 in 50 000 live births across all ethnicities and is more common in females by a 4 3 ratio. Cri du chat syndrome is a rare genetic condition that is caused by the deletion of genetic material on the the p arm of chromosome 5. Symptoms vary greatly from case to case depending upon the exact size and location of the deleted genetic material. There is no specific treatment for cri du chat syndrome.
In these cases the parent carries a chromosomal rearrangement called a balanced translocation in which no genetic material is gained or lost.