Molekulare und genetische Medizin

Pediatric Genomic Medicine in Genetic Diseases of Children

Abstract

Daniel Kysh

Pediatric genomic medicine has revolutionized healthcare by providing insights into the genetic basis of diseases in children. In recent years, the use of genetic testing for ancestry information has become increasingly common in pediatric genomics. These tests can provide valuable insights into a child's genetic heritage and can be used to identify potential disease risks, inform treatment decisions, and facilitate better healthcare outcomes. However, the integration of genetic ancestry findings into pediatric genomic medicine also raises complex ethical, legal and social issues. In this article, we will explore the role of genetic ancestry findings in pediatric genomic medicine, its applications, benefits, and the associated ethical considerations. Genetic ancestry findings, often referred to as genetic ancestry testing or DNA ancestry testing, involve the analysis of an individual's DNA to determine their genetic heritage and ancestry.