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Genetic counseling is recommended for prospective parents with a family history of Gaucher disease. Testing can determine if parents carry the gene that could pass on the Gaucher disease. A prenatal test can also tell if the fetus has Gaucher synd...
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Genetic counseling is advised for individuals with Gaucher disease and for their relatives to accurately assess risk and discuss testing options. For couples who previously had a child with Gaucher or in situations where both parents are carriers ...
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Genetic counseling is advised for individuals with Gaucher disease and for their relatives to accurately assess risk and discuss testing options. For couples who previously had a child with Gaucher or in situations where both parents are carriers ...
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Genetic counseling is advised for individuals with Gaucher disease and for their relatives to accurately assess risk and discuss testing options. For couples who previously had a child with Gaucher or in situations where both parents are carriers ...
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Genetic counseling is a communication process by which personal genetic risk information is translated into practical information for families. Genetic counselors are health care professionals with specialized training and experience in the areas ...
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Genetic counseling aims to facilitate the exchange of information regarding a person's genetic legacy. It attempts to: accurately diagnose a disorder assess the risk of recurrence in the concerned family members and their relatives provide alterna...
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Detailed information on when to seek genetic counseling Genetic counseling is a professional assessment of a person's or couples' risk factors regarding their family history and/or a pregnancy. The goal of genetic counseling is not only risk assessment, but also to explain the cause and inheritance of a disorder, the availability of testing, the prognosis, medical management, and treatment. Genetic counseling sessions typically last one hour or longer, depending upon the complexity of the case.Genetic counseling can be provided by a geneticist, a physician with special training and Board Certification in genetics, or by genetic counselors. Genetic counselors have a minimum of a master's degree in genetic counseling or related field, which includes extensive training in human clinical genetics and counseling. The American Board of Genetic Counseling (ABGC) offers a certification examination for this discipline every three years.
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Genetic counseling is a communication process by which personal genetic risk information is translated into practical information for families. Genetic counselors are health care professionals with specialized training and experience in the areas ...
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Genetic counseling is a communication process by which personal genetic risk information is translated into practical information for families. Genetic counselors are health care professionals with specialized training and experience in the areas ...
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A branch of science that attempts to understand the fundamental biologic makeup of organisms by examining the genetic blueprints in each cell The nucleus of every cell holds the key to nearly every visible and invisible feature of the human body, ...
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Information about a patient's family history is valuable in assessing the risk of mental illness. Within the field of psychiatry, the importance of genetic counseling is growing, but on its own it cannot provide all the answers.
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Antepartum testing involves the use of electronic fetal monitoring (EFM) or ultrasound (US) to assess fetal well-being as determined by the fetal heart rate (FHR) and other characteristics during the antepartal period, which is the period spanning...
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CVS is a test that helps you learn if a fetus has health problems. The test is most often done between weeks 9 and 11 of pregnancy.
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Detailed information on prenatal diagnosis to detect fetal abnormalities in the womb
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Antepartum testing consists of a variety of tests performed late in pregnancy to verify fetal well-being, as judged by the baby's heart rate and other characteristics. Antepartum tests include the nonstress test (NST), biophysical profile, and con...
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Detailed information on biochemical genetic testing Biochemical genetic testing involves the study of enzymes in the body which may be abnormal in some way. They may be deficient or absent, unstable, or have altered activity which can lead to clinical manifestations in a child (i.e., birth defects). These types of disorders are usually called "inborn errors of metabolism" since they are present a birth and affect how the body's metabolism works. Metabolism is a term which describes how the body converts food to energy, and then gets rid of the waste products.
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Detailed information on the uses of genetic testing diagnostic testing
Diagnostic testing is used to identify or confirm the diagnosis of a disease or condition in a person or a family. Diagnostic testing gives a "yes" or "no" answer in most cases. It is sometimes helpful in determining the course of a disease and the choice of treatment. Examples of diagnostic testing include chromosome studies, direct DNA studies, and biochemical genetic testing.
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Detailed information on medical history and genetic testing To evaluate a child for birth defects, healthcare providers not only look at a child's newborn screening test results, but also look at the prenatal history of the mother during the pregnancy with the child, the child's neonatal and pediatric history, and the results of any genetic testing the child has had.
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Determining the correct dosage of warfarin for a heart patient can take several weeks. A company is selling a test that it claims will shorten the process, but there is no evidence yet to support the claim.
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A genetic test examines the genetic information contained inside a person's cells, called DNA, to determine if that person has or will develop a certain disease or could transmit a disease to a child. Genetic tests also determine whether or not co...
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A genetic test examines the genetic information contained inside a person's cells, called DNA, to determine if that person has or will develop a certain disease or could pass a disease to his or her offspring. Genetic tests also determine whether ...
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A genetic test examines the genetic information contained inside a person's cells, called DNA , to determine if that person has or will develop a certain disease or could pass a disease to his or her offspring. Genetic tests also determine whether...
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Genetic testing is a process which involves examining individuals' genetic material for the presence of a change that indicates why they may have developed a disease or disorder. Genetic testing may also tell patients if they are at increased risk...
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A genetic test examines the genetic information contained inside a person's cells, called DNA , to determine if that person has or will develop a certain disease or could pass a disease to his or her offspring. Genetic tests also determine whether...
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Certain inherited genetic conditions increase the risk of cardiovascular disease, so having a genetic test may show whether a person is at risk for heart disease, especially if a family member has one of the conditions.
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