Snijders Blok-Campeau Syndrome

Snijders Blok-Campeau Syndrome

Snijders Blok-Campeau syndrome is a rare genetic disorder characterised by developmental delays, intellectual disability, and distinctive facial features. It results from mutations in the CHD3 gene. Individuals with Snijders Blok-Campeau syndrome often require supportive therapies and personalised care. Early diagnosis is crucial for management and improving quality of life.