Track: Genetics and Genomic Medicine in Pediatrics

Genetics and Genomic Medicine in Pediatrics is a vibrant field that combines genetics, genomics, and pediatric medicine. Its goal is to understand the genetic basis of pediatric disorders and use that information to enhance diagnosis, treatment, and prevention. By understanding the integration of these approaches into clinical practice, attendees will be better prepared to utilize genetic data for diagnosis, management, and personalized treatment, ultimately enhancing patient care and outcomes in pediatrics

Genetic Testing and Counseling in Pediatrics:

This session focuses on the methodologies and applications of genetic testing in pediatric care, including Chromosomal Microarray Analysis (CMA) and Whole-Exome Sequencing (WES). It also covers the role of genetic counseling in interpreting results and guiding families through the implications of genetic findings.

Genomic Approaches to Diagnosing Rare Diseases:

Explore the use of genomic technologies, such as Next-Generation Sequencing (NGS) and Whole-Genome Sequencing (WGS), in diagnosing rare and undiagnosed pediatric diseases. This session highlights the process of integrating genomic data into clinical workflows to improve diagnostic accuracy and patient outcomes.

Cancer Genomics in Pediatrics:

This session examines the role of genomic profiling in pediatric oncology, including tumor genomics and precision medicine approaches. Topics include the use of genomic data to guide targeted therapies and improve treatment strategies for pediatric cancers.

Genetics of Metabolic Disorders:

Focused on the genetic underpinnings of pediatric metabolic disorders, this session covers conditions such as phenylketonuria (PKU) and mucopolysaccharidoses (MPS). It includes discussions on genetic testing, metabolic pathways, and treatment modalities tailored to genetic profiles.

Epigenetics and Pediatric Health:

This session explores the role of epigenetic modifications in pediatric health, including how environmental factors and genetic predispositions influence gene expression. Topics include the impact of epigenetic changes on developmental and chronic conditions in children.

Genomics in Pediatric Cardiology:

Examine the application of genomic medicine in pediatric cardiology, including the identification of genetic mutations associated with congenital heart defects and cardiomyopathies. This session highlights the use of genomic data to personalize treatment and improve cardiovascular outcomes in children.

You may participate in crucial discussions that are shaping the future of pediatrics by submitting your abstract. The advancement of ideas and advancements that will have a long-lasting effect on pediatric care globally can greatly benefit from your involvement. This is your chance to influence the story and help resolve the most pressing problems in the industry.

2nd International Conference on Pediatrics and Child Health

Track: Genetics and Genomic Medicine in Pediatrics

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