Genetics of Cerebral Palsy: Diagnosis, Differential Diagnosis, and Beyond

Abstract excerpt

Cerebral palsy (CP) is the most common motor disability in children, characterized by diverse clinical manifestations and often uncertain etiology, which has spurred increasing interest in genetic diagnostics. This review synthesizes findings from various studies to enhance understanding of CP's genetic underpinnings. The discussion is structured around five key areas: monogenic causes and copy number variants...

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• Cerebral Palsy and Movement Disorders
• Family and Disability Support Research
• Neurogenetic and Muscular Disorders Research