Gabriele de Vries syndrome

Gabriele de Vries syndrome, also known as YY1 haploinsufficiency syndrome, GADEVS, Gabriele-De Vries syndrome, or Gabriele-de Vries syndrome, is a rare condition. It is linked to changes affecting the YY1 gene, which plays an important role in normal development. The available information on this condition is limited, and details about how it presents in people are still being explored. Because this syndrome is rare, studies and detailed descriptions of its features are still evolving. Researchers and clinicians continue to collect data to better understand how changes in the YY1 gene may influence development and overall health in people with the condition.

Information about symptoms is currently limited for this condition.

Gabriele de Vries syndrome is associated with haploinsufficiency of the YY1 gene, meaning that having only one functional copy of this gene may contribute to the condition. This genetic factor is considered a primary cause, although detailed mechanisms and additional risk factors are not well defined at this time.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.