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Genetic counseling and Triple test

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Genetic counseling and Triple test

Genetic counseling vs. Triple test

Genetic counseling is the process by which the patients or relatives at risk of an inherited disorder (or may be carrying a child at risk) are advised of the consequences and nature of the disorder, the probability of developing or transmitting it, and the options open to them in management and family planning. The triple test, also called triple screen, the Kettering test or the Bart's test, is an investigation performed during pregnancy in the second trimester to classify a patient as either high-risk or low-risk for chromosomal abnormalities (and neural tube defects).

Similarities between Genetic counseling and Triple test

Genetic counseling and Triple test have 9 things in common (in Unionpedia): Amniocentesis, Cell-free fetal DNA, Chorionic villus sampling, Down syndrome, Edwards syndrome, Nuchal scan, Patau syndrome, Prenatal testing, Ultrasound.

Amniocentesis

Amniocentesis (also referred to as amniotic fluid test or AFT) is a medical procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections, and also for sex determination, in which a small amount of amniotic fluid, which contains fetal tissues, is sampled from the amniotic sac surrounding a developing fetus, and then the fetal DNA is examined for genetic abnormalities.

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Cell-free fetal DNA

Cell-free fetal DNA (cffDNA) is fetal DNA which circulates freely in the maternal blood.

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Chorionic villus sampling

Chorionic villus sampling (CVS), sometimes called "chorionic villous sampling" (as "villous" is the adjectival form of the word "villus"), is a form of prenatal diagnosis to determine chromosomal or genetic disorders in the fetus.

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Down syndrome

Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21.

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Edwards syndrome

Edwards syndrome, also known as trisomy 18, is a genetic disorder caused by the presence of all, or part of a third copy of chromosome 18.

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Nuchal scan

A nuchal scan or nuchal translucency (NT) scan/procedure is a sonographic prenatal screening scan (ultrasound) to detect cardiovascular abnormalities in a fetus, though altered extracellular matrix composition and limited lymphatic drainage can also be detected.

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Patau syndrome

Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13.

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Prenatal testing

Prenatal testing consists of prenatal screening and prenatal diagnosis, which are aspects of prenatal care that focus on detecting problems with the pregnancy as early as possible.

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Ultrasound

Ultrasound is sound waves with frequencies higher than the upper audible limit of human hearing.

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The list above answers the following questions

Genetic counseling and Triple test Comparison

Genetic counseling has 45 relations, while Triple test has 36. As they have in common 9, the Jaccard index is 11.11% = 9 / (45 + 36).

References

This article shows the relationship between Genetic counseling and Triple test. To access each article from which the information was extracted, please visit:

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