8q24.3 microdeletion syndrome

8q24.3 microdeletion syndrome, also known as Verheij syndrome, VRJS, or chromosome 8Q24.3 deletion syndrome, is a rare genetic condition associated with a small deletion on chromosome 8. This deletion affects a region of the chromosome that includes the gene PUF60. Detailed descriptions of this condition are still emerging, and the overall picture of its clinical presentation remains under study.

Information about symptoms is currently limited for this condition.

This condition is associated with a microdeletion on part of chromosome 8, specifically in the q24.3 region. The deletion affects the PUF60 gene, which may play a role in development. However, further research is needed to fully understand how this genetic change leads to the condition.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research is currently limited for this condition.