Pediatric Neurology: Genetic, Developmental & Rare CNS Conditions
Pediatric CNS disorders represent a highly diverse spectrum of genetic, developmental, metabolic, and neurodegenerative conditions affecting infants and children. Advances in genomic technologies allow precise identification of rare mutations, channelopathies, metabolic errors, and chromosomal anomalies underlying many pediatric neurological disorders. Early recognition of developmental delays, neuromuscular abnormalities, epilepsy syndromes, and neurobehavioral phenotypes is essential for effective intervention. Modern therapies incorporate gene editing, antisense oligonucleotides, metabolic correction strategies, targeted pharmacology, and advanced rehabilitation approaches tailored to pediatric needs. Neurodevelopmental plasticity offers unique opportunities for early therapeutic impact, making timely diagnosis and precision-guided treatment critical. Multidisciplinary care models including neurology, genetics, physiotherapy, behavioral sciences, and nutrition support broader functional development and improved long-term quality of life.
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