Patient's Treatment Reports
Rare, severe epilepsy syndrome in infants characterized by spasms, hypsarrhythmia, and developmental delay.
Spinal Muscular Atrophy
Inherited disease that causes muscle weakness and wasting.
Global Development Delay
Significant delay in a child’s physical, cognitive, and social-emotional development.
Attention-deficit/Hyperactivity Disorder (ADHD)
Neurodevelopmental disorder characterized by inattention, hyperactivity, and impulsivity.
Dyspraxia is a developmental coordination disorder that affects movement, coordination, and balance.
Genetic disorder caused by an extra chromosome 21, leading to mild to moderate intellectual disability.
Dyslexia is a learning difficulty that affects reading, writing, and spelling.