What types of genetic testing exist, in what situations is each used, and how can a person, given their personal or family history of illness, understand which type of test will be most informative and useful for diagnosis, prevention, or treatment planning?

Genetic testing includes various types: diagnostic tests confirm a condition if symptoms appear; presymptomatic tests assess risk based on family history before symptoms; carrier screening identifies if you can pass genetic conditions to children; pharmacogenetic tests help personalize medication plans; prenatal and newborn screenings detect conditions early. Choosing the right test depends on personal and family history and goals. Consulting a genetic counselor is essential to determine the most useful option. More details at https://globalmedik.com/e...whether-you-should-do-it/ .