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Genetic screening Uses Carrier screening Screening pre-implantation embryos Prenatal diagnostic screening Newborn screening Pre-symptomatic screening in adults Confirming diagnosis © 2010 Paul Billiet ODWS Tests Over 1000 tests available Alzheimer's disease* (APOE; late-onset variety of senile dementia) Inherited breast and ovarian cancer* (BRCA 1 and 2; early-onset tumors of breasts and ovaries) Hereditary nonpolyposis colon cancer* (CA; early-onset tumors of colon and sometimes other organs) Cystic fibrosis (CF; disease of lung and pancreas resulting in thick mucous accumulations and chronic infections) Hemophilia A and B (HEMA and HEMB; bleeding disorders) Huntington's disease (HD; usually midlife onset; progressive, lethal, degenerative neurological disease) Phenylketonuria (PKU; progressive mental retardation due to missing enzyme; correctable by diet) Sickle cell disease (SS; blood cell disorder; chronic pain and infections) © 2010 Paul Billiet ODWS Gene probes Short pieces of DNA or RNA (100 – 1000 bases) complementary to a given sequence of nucleotides Target DNA denatured (strands separate) Probe added and binds to complementary sequence Radioactive marker attached to probe so it can be identified © 2010 Paul Billiet ODWS FISHing for genes FISH = Fluorescent In Situ Hybridisation Used to identify chromosomal abnormalities and mapping chromosomes Image Credit: Journal of Medical Gdenetics FISH analysis of a chromosome abnormality where material is switched between chromosomes 9 and 11 Pros Identifying potential parents of affected children Identifying pre-symptomatic adults © 2010 Paul Billiet ODWS Cons Lab errors (false positives/false negatives) Uncertainties in diagnosis from positive result Lack of medical treatment in case of positive test Risk of discrimination © 2010 Paul Billiet ODWS