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ISSN: 2572-4983

Neonatal and Pediatric Medicine
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  • Brief Report   
  • Neonat Pediatr Med 10: 446,

Genetic Disorders in Pediatrics: Understanding Causes, Diagnosis, and Management

Fatima Zahedi*
Department of Medical Biotechnology and Nanotechnology, Mashhad University of Medical Sciences, Iran
*Corresponding Author : Fatima Zahedi, Department of Medical Biotechnology and Nanotechnology, Mashhad University of Medical Sciences, Iran, Email: fatima@gmail.com

Received Date: Aug 02, 2024 / Published Date: Aug 28, 2024

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

Citation: Fatima Z (2024) Genetic Disorders in Pediatrics: Understanding Causes, Diagnosis, and Management. Neonat Pediatr Med 10: 446.

Copyright: © 2024 Fatima Z. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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