yes
yes
Prenatal tests for Cat Eye Syndrome (CES) typically involve genetic testing and imaging techniques. Chorionic villus sampling (CVS) or amniocentesis can be performed to analyze fetal chromosomes for the presence of abnormality associated with CES. Additionally, ultrasound may be used to identify physical anomalies that could suggest the syndrome. Genetic counseling is also recommended for parents with a family history of CES or other chromosomal abnormalities.
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
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.