Medical EditorDr. Nicholas Bush MBBS BSc (Hons)
2 min read
Last Updated: 8 August 2024
Weaver Syndrome
Medical EditorDr. Nicholas Bush MBBS BSc (Hons)
2 min read
Last Updated: 8 August 2024
Weaver Syndrome
Weaver syndrome is a rare genetic disorder characterised by rapid growth in infancy, skeletal abnormalities, and distinctive facial features. Caused by mutations in the EZH2 gene, it also includes developmental delays and increased risk of neoplasms. Early diagnosis of Weaver syndrome is crucial for managing symptoms and providing appropriate care.
Trusted Resources

National Institute of Health (NIH)
Weaver Syndrome