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  2. Genetic testing - Wikipedia

    en.wikipedia.org/wiki/Genetic_testing

    Genetic testing, also known as DNA testing, is used to identify changes in DNA sequence or chromosome structure. Genetic testing can also include measuring the results of genetic changes, such as RNA analysis as an output of gene expression, or through biochemical analysis to measure specific protein output. [1]

  3. Carrier testing - Wikipedia

    en.wikipedia.org/wiki/Carrier_testing

    Carrier testing is a type of genetic testing that is used to determine if a person is a carrier for specific autosomal recessive diseases. [1] This kind of testing is used most often by couples who are considering becoming pregnant to determine the risks of their child inheriting one of these genetic disorders. [2]

  4. Elective genetic and genomic testing - Wikipedia

    en.wikipedia.org/wiki/Elective_genetic_and...

    Family sharing. The implications of genetic test results for other family members are important to consider in patients considering elective genetic testing. Unlike most other medical tests, genetic testing may reveal health information about the patient as well as his or her family members. [51]

  5. Color's new DNA test kit can identify inherited heart conditions

    www.aol.com/news/2018-03-20-colors-dna-test-kit...

    Genetic testing company Color is mostly known for its DNA tests for cancer, but its most recent test kit is all about the heart. Color's new kit can detect predispositions to various inherited ...

  6. Genetic counseling - Wikipedia

    en.wikipedia.org/wiki/Genetic_counseling

    A genetic counsellor discussing a pedigree with a client. Genetic counseling is the process of investigating individuals and families affected by or at risk of genetic disorders to help them understand and adapt to the medical, psychological and familial implications of genetic contributions to disease.

  7. Familial dysautonomia - Wikipedia

    en.wikipedia.org/wiki/Familial_dysautonomia

    If both parents are carriers, a one in four chance exists with each pregnancy for an affected child. Genetic counseling and genetic testing are recommended for families who may be carriers of familial dysautonomia. [13] Worldwide, about 600 diagnoses have been recorded since discovery of the disease, with around 350 of them still living. [17]

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