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Do dogs get genetic disorders?
Yes. Dogs (and every other species with DNA) can get a genetic disorder. This can be due to inheriting a disorder from a parent, or by a copying error from a parent, such as a mutation or a DNA sequence being dropped, duplicated, reversed, etc. Of course, we know much more about human genetic disorders than dog disorders. Sometimes a "disorder" is actually an advantage under some circumstances, which explains why some disorders are preserved through history, such as sickle-cell anemia in humans (helps one survive malaria).
What is a substance that scientists can produce through genetic engineering?
Insylin has been produced through genetic engineering.
What is most a benefit of genetic engineering?
production of human insulin through genetic modification of bacterial genes
What is most clearly a benefit of genetic engineering?
production of human insulin through genetic modification of bacterial genes
What are the Social issues relating genetic engineering?
there are many issues dealing with genetic engineering, most people who go through genetic therapy come out with a disease, when they didn't before
Can Marfan Syndrome be detected before birth?
Yes, Marfan Syndrome can be detected before birth through prenatal genetic testing such as chorionic villus sampling or amniocentesis. These tests can detect whether the fetus has inherited the genetic mutation that causes Marfan Syndrome. It's important to consult with a genetic counselor or healthcare provider for further information and testing options.
Can Achondroplasia be detected before birth?
Yes, it can be detected before birth. Doctors can use an ultrasound to determine if the child is homozygous dominant or heterozygous, in which cases the child would be infected with Achondroplasia, because it is a dominant trait.
What are the causes of genetic human disorders?
The causes of genetic disorders areThey can be inherited through Parents;Mutations may occur;A deletion may occur.These are the causes of a genetic disorder.
What is name of the procedure that remove and test amniotic fluid?
The procedure that removes and tests amniotic fluid is called amniocentesis. During this procedure, a thin needle is inserted through the abdominal wall into the uterus to extract a small amount of amniotic fluid, which contains fetal cells. This fluid is then analyzed for genetic disorders, infections, or other conditions affecting the fetus. Amniocentesis is typically performed during the second trimester of pregnancy.
What can be tested out on fetuses?
Fetuses can be tested for various genetic and chromosomal conditions through procedures like amniocentesis and chorionic villus sampling (CVS). These tests can identify conditions such as Down syndrome, cystic fibrosis, and certain metabolic disorders. Additionally, non-invasive prenatal testing (NIPT) can assess the risk of genetic disorders using a sample of the mother's blood. However, ethical considerations and potential risks associated with these procedures are important factors in decision-making.
What does diagnostic amniocentesis include?
Diagnostic amniocentesis is a medical procedure used to obtain amniotic fluid for testing, typically performed during the second trimester of pregnancy. The procedure involves inserting a thin needle through the abdominal wall and into the uterus to collect the fluid, which contains fetal cells and various substances. The collected fluid can then be analyzed for genetic disorders, chromosomal abnormalities, and other conditions affecting the fetus. It is usually recommended when there is an increased risk of genetic issues based on maternal age, family history, or abnormal screening results.
How are genetic disorders reconized?
through DNA testing and physical and/or behavioral analysis
Genetic disorders are caused by?
Genetic disorders are caused by abnormalities in an individual's DNA, either through mutations or changes in the genes. These abnormalities can be inherited from parents or can occur spontaneously during a person's lifetime. Genetic disorders can affect various aspects of health and development.
Can jacobsen syndrome be detected prenatally?
Yes, Jacobsen syndrome can potentially be detected prenatally through genetic testing methods such as chorionic villus sampling (CVS) or amniocentesis, which analyze the fetus’s chromosomes for abnormalities. Non-invasive prenatal testing (NIPT) can also assess the risk of chromosomal conditions, although it may not specifically identify Jacobsen syndrome. Early ultrasounds may reveal certain physical anomalies associated with the condition, but definitive diagnosis typically requires genetic analysis.
Can cri du chat be detected before birth?
Yes, cri du chat syndrome can potentially be detected before birth through prenatal genetic testing. Non-invasive prenatal testing (NIPT) and invasive procedures like amniocentesis or chorionic villus sampling (CVS) can identify chromosomal abnormalities associated with the syndrome. However, these tests are not routinely performed unless there are specific risk factors. Ultimately, genetic counseling is recommended for expecting parents to understand the implications and options available.
Can you get a genetic disorder from catching a cold from an infected person?
No. Genetic disorders are rooted in the DNA of the body and can only be transmitted through heredity.
What withdrawl of tissue from the placenta?
Withdrawal of tissue from the placenta, commonly referred to as placental tissue sampling, is a diagnostic procedure used to obtain cells for genetic analysis or to assess the health of the fetus. This can be performed through methods such as chorionic villus sampling (CVS) or amniocentesis, depending on the timing and specific circumstances. The collected tissue can help identify chromosomal abnormalities, genetic disorders, or infections, providing critical information for prenatal care.
