22q11.2 distal deletion syndrome is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22.

DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22.

A 22q11.2 distal deletion is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22. For ...

22q11.2 duplication syndrome is a rare genetic disorder caused by a duplication of a segment at the end of chromosome 22.

May 9, 2024 · 22q11.2DS is an autosomal dominant contiguous gene deletion syndrome. In 22q11.2DS caused by a 3.0 (2.54)-Mb deletion, the deletion is de novo in more than 90% ...

Dec 1, 2019 · 22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22.

Jan 13, 2024 · DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a condition caused when a small part of chromosome 22 is missing.

Jul 26, 2023 · 22q11.2DS is a disorder caused by a small piece of chromosome 22 missing. 22q11.2DS is associated with a range of problems including: congenital heart disease.