Rett Syndrome
Rett syndrome is a rare genetic disorder that almost exclusively affects girls, becoming apparent between 6 to 18 months of age, and leads to severe nervous system and developmental issues, including loss of speech, motor skills, coordination, and behavioral capabilities. Complications can include seizures, scoliosis, and sleep disturbances, and the severity of symptoms varies among individuals.
Health Outcomes
- Improved Child Neurodevelopment
- Improved Child Neurodevelopment (Adaptive Domain)
- Improved Child Neurodevelopment (Motor Domain)
- Improved Child Neurophysiological Outcome
- Improved Developmental Milestone
- Improved Gross Motor Function
- Improved Intellectual Disability
- Improved Language Development
- Improved Language Score
- Improved Mental Developmental Quotient
- Improved Motor Function
- Improved Neurodevelopmental Performance
- Improved Performance Developmental Score
- Improved Personal-Social Developmental Score
- Increased Head Circumference
- Prevented Neurometabolic Decline
- Reduced Aberrant Behavior Checklist Score
- Reduced Adverse Neurodevelopmental Outcome
- Reduced Cytoskeleton Disruption
- Reduced Individual Variability
- Reduced Repetitive Behaviors
- Reduced Self-Injurious Behavior
- Reduced Stereotypic Behavior