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is a rare condition caused by short arm and a small section of the long arm of human chromosomes.

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A diagnosis of cat eye syndrome is often suspected based on the presence of characteristic signs and symptoms. Also missing chromosomes.

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In people affected by cat eye syndrome, each cell has at least one small extra duplicate chromosome made up of a genetic.

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Around 1 out of 50,000 to one of out 150,000 people in the general population have cat eye syndrome.

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iris coloboma

opening to the anus is missing

Skin tags or pits in front of the ears

Unusually shaped ears

hearing loss

widely spaced eyes

outside corners of the eyes point downward)

Strabismus

Congenital heart defects

urinary problems

Skeletal abnormalities

Developmental delay

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Most cases of cat eye syndrome are not inherited. The condition generally occurs fast as a random event during the formation of the egg or sperm. The person would have no family history of the condition but could pass it on to their children

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Treatment for this condition varies based on the signs and symptoms in each person.

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urinary tract kidenyees