|deletion of 5p||1.81||0.7||8821||75|
22q11.2 deletion syndrome is caused by a missing piece (deletion) of part of chromosome 22 in each cell. The deletion occurs near the middle of the chromosome on the q arm at a location known as q11.2.What is 5p syndrome?
Cri du chat syndrome, also known as 5p- (5p minus) syndrome or cat cry syndrome, is a genetic condition present from birth that is caused by the deletion of genetic material on the small arm (the p arm) of chromosome 5.   Infants with this condition often have a high-pitched cry that sounds like that of a cat.What is chromosome 7p deletion syndrome?
Summary Summary. Listen. Chromosome 7p deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) of chromosome 7. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved.What is a deletion syndrome?
1p36 deletion syndrome is a disorder that typically causes severe intellectual disability. Most affected individuals do not speak, or speak only a few words. They may have temper tantrums, bite themselves, or exhibit other behavior problems.