Cat Eye Syndrome (CES) is a rare genetic disorder that can affect individuals regardless of gender or ethnicity. It is typically caused by a chromosomal anomaly, specifically involving the 22nd chromosome. While anyone can theoretically be a candidate, the syndrome is most often diagnosed in children and is associated with various physical, developmental, and health-related features. Genetic counseling may be beneficial for those with a family history or concerns about the condition.
The abnormalities common to cat eye syndrome were first cataloged in 1898 in Germany.
Cat eye syndrome was first described in 1969 by scientists at the Johns Hopkins Hospital in Baltimore, led by Dr. Alfred Knudson. They named the syndrome after the striking feature of vertical colobomas in the eyes that resemble a cat's eye.
no
Black people get cat eye syndrome more easily than any other race
yes
Cat eye syndrome is also known as Schmid-Fraccaro syndrome and is sometimes referred to by its genetic designation, 22q11.2 deletion syndrome. This condition is characterized by various physical abnormalities, including eye defects that resemble a cat's eye. The name reflects the distinctive appearance of the eyes, but it can also be associated with other features and health issues.
Autosomal Dominant
I don't think it can. Because it is a birth defect
I don't think it can. Because it is a birth defect
whats affected is the right to see
Cat eye syndrome is a genetic condition that is caused by an extra piece of genetic material on chromosome 22. It is not determined by simple dominant or recessive inheritance patterns, but rather by the presence of the extra genetic material.
A partial trisomy or tetrasomy of the top part of chromosome 22 in proximal 22q11