Abstract

Pediatric genetic disorders are a diverse group of conditions resulting from alterations in genes or chromosomes, which can lead to a wide range of health issues. These disorders can manifest as developmental delays, metabolic imbalances, or physical anomalies, among other symptoms. The early identification of genetic disorders is essential for prompt intervention and management, which can significantly improve the quality of life of affected children. This article provides an overview of the most common pediatric genetic disorders, their causes, diagnosis, and management strategies. Advances in genetic testing, personalized treatments, and the role of genetic counseling are also discussed