Cri du Chat syndrome is characterized by a distinct high-pitched, cat-like cry in infancy, which is due to a deletion on chromosome 5. Other associated features include developmental delays, intellectual disabilities, microcephaly, and distinctive facial features such as a broad nasal bridge and widely spaced eyes. Individuals may also experience hypotonia (low muscle tone) and have a higher incidence of certain medical issues, such as heart defects. Early intervention and supportive therapies can help improve outcomes for those with the disorder.
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