Other symptoms of cri du chat syndrome may include:

For example, Cri du chat syndrome involves a deletion on the short arm of chromosome 5.

Genetic counseling and genetic testing may be offered to families with individuals who have cri du chat syndrome.

Cri du chat syndrome is due to a partial deletion of the short arm of chromosome number 5, also called "5p monosomy".

Luchsinger published more than 120 research articles, ranging in topic from Cri Du Chat Syndrome to laryngeal surgery.

These abnormalities include what has been called the cri du chat syndrome, which results from the loss of the tip of another type of chromosome, chromosome 5.

Cri du chat Syndrome (CdCS) is a complex disorder involving the loss of the distal portion of the short arm of chromosome 5.

The deletion of the telomerase reverse transcriptase (hTERT) gene localized in 5p15.33 may contribute to the phenotypic changes in cri du chat syndrome as well.

Deletion of this area of chromosome 5 is associated with mental retardation, psychotic behavior, autism, macrocephaly and hypernasal-like speech, as well as the disorder Cri du chat syndrome.

Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p minus syndrome or Lejeune's syndrome, is a rare genetic disorder due to a missing part of chromosome 5.