Weaver syndrome is an extremely rare autosomal dominant genetic disorder associated with rapid growth beginning in the prenatal period and continuing through the toddler and youth years.

Aug 30, 2022 · Weaver syndrome is a rare genetic condition that causes tall stature. It can also cause facial differences, intellectual disabilities and problems with bones, joints and muscles.

Weaver syndrome is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur …

Nov 18, 2021 · Learn about Weaver Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find resources and.

Jul 20, 2025 · Weaver syndrome is a rare, congenital genetic condition characterized by accelerated growth. This rapid growth often begins before birth, causing children to be significantly taller and …

Children born with Weaver Syndrome are likely to encounter a number of additional symptoms, aside from the overgrowth. These include a curving of the upper back, heart defects, flat feet, weak muscle …

Here you’ll find comprehensive resources to support you and your loved ones in navigating life with Weaver syndrome. Connect with support networks and self-help groups for people living with …