is a genetic disorder caused by a small deletion in chromosome 22 at position q11.2. The condition is usually not passed on from parents to the child except in some cases. Most cases occur ...

Researchers have identified a promising strategy to improve memory and brain cell function in models of 22q11.2 Deletion ...

Many important clinical conditions like Down syndrome and chronic myelogenous ... and numbered 1 to 22. The last pair is the sex chromosomes (X and Y). Each chromosome has two arms, named p ...

One person in 2000 suffers from a microdeletion of chromosome 22 that can lead to the development of psychotic disorders, such as schizophrenia, in adolescence. In addition to symptoms such as ...

The unstable part of chromosome 22 is important in the formation of organs and also in relation to learning and behaviour disorders. "Its early identification is vital. If we can recognise ...

DiGeorge syndrome, a 22q11.2 deletion syndrome, is caused when a small portion of chromosome 22 is missing. The condition can ...

Phelan-McDermid syndrome is a rare genetic condition impacting speech, mobility, and cognitive development. It typically occurs due to an alteration in chromosome 22 and is present from birth.

The UCLA study examined a particular genetic condition called chromosome 22q11.2 deletion syndrome—caused by missing DNA on chromosome 22—which is associated with a higher risk of developing ...

Trisomy 18 is a condition caused by a problem in your chromosomes. It's also called Edwards syndrome, after the doctor who first described it. Chromosomes are the threadlike structures in cells ...