22q11.2 deletion syndrome
22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a constellation of findings due to a deletion in 22q11.2.
It is characterized by hypoplasia of the:[1]
22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a constellation of findings due to a deletion in 22q11.2.
It is characterized by hypoplasia of the:[1]