DiGeorge syndrome, additionally referred to as chromosome 22q11.2 deletion syndrome, is a genetic situation that leads to developmental issues in lots of the physique’s techniques. A small deletion on chromosome 22 causes the syndrome. Because of this a small portion of chromosome 22 is lacking.
DiGeorge syndrome is uncommon, affecting between 1 in 3,000 to 1 in 6,000 births.
Right here’s what you want to find out about DiGeorge syndrome, the way it might have an effect on your youngster, and what the outlook is as your youngster grows into maturity.
The deletion of a particular a part of chromosome 22 referred to as q11.2 causes DiGeorge syndrome. That lacking piece of DNA normally comprises about 30 to 40
genes. The lacking genes may cause varied bodily and neurodevelopmental circumstances.