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Parents with a family history of congenital adrenal hyperplasia(of any type) or a child who has the condition should consider genetic counseling.Prenatal diagnosis is available for some forms of congenital adrenal hyperplasia. Diagnosis is made in...
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A person who has a relative with CAH or parents who have a child with CAH21 should consider undergoing carrier testing. Carriers for CAH21 can sometimes be identified through the ACTH stimulation test, although DNA testing is more accurate and is...
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Prenatal therapy, in which a pregnant woman at risk for a second CAH child is given dexamethasone to decrease secretion of androgens by the adrenal glands of the female fetus, has been in use since 1994. This therapy is started in the first trime...
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Prenatal therapy, in which a pregnant woman at risk for a second CAH child is given dexamethasone to decrease secretion of androgens by the adrenal glands of the female fetus, has been in use for about 10 years. This therapy is started in the fir...
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A person who has a relative with CAH or parents who have a child with CAH21 should consider undergoing carrier testing. Carriers for CAH21 can sometimes be identified through the ACTH stimulation test, although DNA testing is more accurate and is...
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The pregnancy is continued if the fetus is disease-free.If a genetic defect is found in the fetus, parents who decide to continue the pregnancy may be better prepared to care for the infant by educating themselves about the disease in advance. For...
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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:.assess the risk of recurrence in the concerned family members and their relatives.provide support groups that will help family m...
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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 fr...
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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 cont...
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