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Results 1 - 10 of 10 for "s:" Birth Defects
  1. ... must be enough fetal cfDNA in the mother’s bloodstream to be able to identify fetal chromosome abnormalities. The proportion of cfDNA in maternal blood that ...
  2. ... some cases, prenatal testing can lessen a couple's uncertainty or help them make decisions about a pregnancy. It cannot identify all possible inherited disorders and birth defects, however. Preimplantation testing Preimplantation testing, also called preimplantation ...
  3. ... A negative screening test means that a person’s risk is lower than average. ... abnormality when the person is actually unaffected (false positive), ...
  4. ... A child with a known inherited disorder, a birth defect, intellectual disability, or ... ethnic background . People related by blood (for example, ...
  5. ... or missing chromosome in each of the body’s cells. Changes in chromosome ... abnormality may want to talk with a genetics professional . ...
  6. ... s dermatoglyphs to be different from everyone else’s. Even identical ... with other abnormalities of the skin. Adermatoglyphia is caused by mutations ...
  7. ... or more genes, or all of a person’s DNA (which is known as their genome). ... proteins or enzymes; abnormalities in either can indicate changes to the DNA ...
  8. ... increased risk of cancerous tumors), are associated with abnormalities of imprinted genes on the short arm of ...
  9. ... proteins or enzymes that are produced from genes. Abnormalities in these substances can indicate that there are ...
  10. ... by disorder and are specific to an individual's health needs. For example, a genetic disorder associated ... therapy . This experimental technique involves changing a person's genes to prevent or treat a disease. Gene ...