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. This deletion causes several body …

DiGeorge syndrome is inherited in an autosomal dominant pattern. DiGeorge syndrome is caused by a heterozygous deletion of part of the long arm (q) of chromosome 22, region 1, band 1, …

Nov 14, 2025 · DiGeorge syndrome (22q11.2 deletion syndrome) is a genetic condition that occurs when your child is missing a piece of chromosome 22. The condition can affect many …

22q11.2 deletion syndrome (22q11.2DS), also known as DiGeorge syndrome, is a genetic disorder that occurs when a small piece of one of the baby’s chromosomes – chromosome 22 …

Jun 5, 2025 · DiGeorge syndrome is a disorder due to a deletion from the 22nd chromosome. Learn about the causes, symptoms, and treatment.

22q11.2 deletion syndrome has many possible signs and symptoms that can affect almost any part of the body. The features of this syndrome vary widely, even among affected members of …

In ~15% of cases, the deletion is nested within the 3 Mb DiGeorge critical region and varies in size. Most deletions include the TBX1 gene that has been shown to be implicated in cardiac, …

Find out about DiGeorge syndrome (22q11 deletion), including why it happens and what problems it can cause.

In children with this syndrome, a tiny piece of one of the copies of chromosome 22 is missing. This can cause many health problems. These problems may range from heart defects and …

DiGeorge syndrome (DGS) is one of a group of phenotypically similar disorders, including velocardiofacial syndrome (VCFS, or Shprintzen syndrome) and conotruncal anomaly face …