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  2. 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.

  3. Galactosialidosis - Wikipedia

    en.wikipedia.org/wiki/Galactosialidosis

    Because the disease is genetically inherited, the only prevention available for this condition is through genetic carrier screening that can detect the presence of a recessive, mutated CTSA gene in parents before they decide to have children. If both parents are found to be carriers of the mutated gene, there will be a 25% possibility of the ...

  4. Natera - Wikipedia

    en.wikipedia.org/wiki/Natera

    Natera, Inc. is a clinical genetic testing company based in Austin, Texas that specializes in non-invasive, cell-free DNA (cfDNA) testing technology, with a focus on women’s health, cancer, and organ health. Natera’s proprietary technology combines novel molecular biology techniques with a suite of bioinformatics software that allows ...

  5. Elective genetic and genomic testing - Wikipedia

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

    Carrier testing is used to identify people who carry one copy of a gene change (also referred to as a variant or mutation) that, when present in two copies, causes a genetic disorder. Carrier testing is typically offered to individuals who are considering pregnancy or are already pregnant, have a family history of a specific genetic disorder ...

  6. X-linked genetic disease - Wikipedia

    en.wikipedia.org/wiki/X-linked_genetic_disease

    Genetic screening including carrier screening, prenatal screening and newborn screening could be done on individuals for early detection of genetic defects. As there are many X-linked genetic diseases, the pathology and mechanism of each varies significantly, there is no clear-cut diagnosis and treatment for all diseases.

  7. MUTYH-associated polyposis - Wikipedia

    en.wikipedia.org/wiki/MUTYH-associated_polyposis

    To identify risk for future offspring, screening should be offered to spouses of individuals affected by MUTYH-associated polyposis. [3] If the spouse is a carrier of a mutation in MUTYH, then genetic counseling should be offered to the children as they approach adulthood. [citation needed]

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  9. American College of Medical Genetics and Genomics - Wikipedia

    en.wikipedia.org/wiki/American_College_of...

    The ACMG, incorporated in 1991, stated mission to give national representation to providers of genetic services and their patients with genetic disorders; to provide education and resources for the medical genetics profession; to improve the health of the public by promoting the development and implementation of methods to diagnose, treat and prevent genetic disease.