Oct 27, 2025
Rett Syndrome is a rare genetic neurological disorder that primarily affects girls, leading to developmental delays, loss of motor skills, and speech difficulties.
Source: unsplash
Most cases are caused by mutations in the MECP2 gene, which affects brain development and function.
Source: unsplash
Repetitive hand movements, breathing irregularities, seizures, and mobility challenges are hallmark symptoms of Rett Syndrome.
Source: unsplash
While intellectual disability varies, children with Rett Syndrome require lifelong care, therapy, and support for daily activities.
Source: unsplash
Diagnosis is based on clinical evaluation and genetic testing. There is no cure, but therapies and medications help manage symptoms.
Source: unsplash
Symptoms may appear between 6 to 18 months and include slowed growth, reduced eye contact, and loss of purposeful hand movements.
Source: unsplash
Spread awareness, support research organizations, and participate in Rett Syndrome events to make a difference.
Source: unsplash
Awareness campaigns, research funding, and community support help families cope and advance scientific understanding.
World Polio Day 2025: Eradication and Prevention of Polio