Most children (90%) with 22q deletion experience some degree of developmental disability with delayed speech and language development as the most consistent ...

Studies show that kids with 22q experience anxiety in everyday situations, even though they might not show the typical signs of distress that teachers will ...

The 22q11.2 deletion syndrome is a genetic disorder caused by a missing section (microdeletion) of chromosome 22, which is present from the time a child is ...

8 days ago · The International 22q11.2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by chromosome 22q11.2 ...

22q11.2 deletion syndrome is a genetic condition that affects many parts of the body. It can cause intellectual disability, learning and social challenges.

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.

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% ...

GeneReviews · Genes and Databases]. · Table 2. [Cardiac Findings in...

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.