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 Developmental Milestone
- Improved Gross Motor Function
- Improved Mental Developmental Quotient
- Improved Motor Function
- Improved Performance Developmental Score
- Improved Personal-Social Developmental Score
- Increased Head Circumference
- Prevented Neurometabolic Decline
- Reduced Cytoskeleton Disruption
- Reduced Repetitive Behaviors
- Reduced Stereotypic Behavior