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

Signs and symptoms · Genetics · Diagnosis · Treatment

2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. The symptoms are caused by the lack of those genes. DiGeorge ...

2 deletion syndrome commonly have congenital heart defects, in particular truncus arteriosus and tetralogy of Fallot, as well as facial abnormalities such as ...

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.

Presentation · Cause · Research

This video discusses the pathophysiology and important signs and symptoms of DiGeorge syndrome. Resources: https://en.wikipedia.org/wiki/DiGeorge_syndrome http ...

DiGeorge syndrome (DGS) is a congenital disorder with a broad phenotypic presentation, which results predominantly from the microdeletion of chromosome 22 at a ...

Jan 13, 2024 · This condition is due to missing part of chromosome 22. It may cause heart issues, thyroid problems, cleft palate, lower immunity and other ...

DiGeorge syndrome (22q11.2 deletion syndrome) is a genetic condition that affects several parts of your body. A missing piece of chromosome 22 causes it.