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Articles in Genetic testing

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Can NIPT test detect thalassemia in 9 weeks fetus?
Doctor, can the NIPT test detect the possibility of Thalassemia in a 9-week-old fetus?
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Pathogenesis and pathogenesis of esophageal eosinophilia in response to anti-acid secretion
Eosinophils are one of the components of white blood cells produced in the bone marrow and are one of the cells that play a role in promoting inflammation, especially allergic inflammatory reactions. Therefore, large quantities of eosin can accumulate in tissues such as the esophagus, stomach, small intestine and sometimes in the blood when such individuals are exposed to the allergen.
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Similarities and differences between PPI-responsive esophageal eosinophilia and eosinophilic esophagitis
Eosinophilic esophagitis (EoE) is an immune-mediated clinical condition presenting with symptoms of esophageal dysfunction and esophageal eosinophilia. Because of the presence of eosinophilia and response to PPI therapy, GERD and PPI-REE have become the most common alternative diagnoses for EoE.
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History of finding esophageal eosinophilia responsive to proton pump inhibitors
Proton pump inhibitor-responsive eosinophilia should be suspected if esophageal symptoms and eosinophil histological findings demonstrate a symptomatic and histological response to proton pump inhibitors.
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What is genetic screening before embryo transfer? Why does it need to be done?
In the process of infertility treatment, genetic diagnosis and testing before embryo transfer is one of the necessary tasks to improve the effectiveness of reproductive health care, support infertility treatment for families or limit the risk of giving birth to children with genetic diseases.
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What you need to know about carrier testing
Having children at the age of 35 or older often has a high risk of fertility problems. Carrier testing is considered an optimal solution to help couples who want to have children reduce their anxiety about this issue.
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The role of genetic testing
Genetic testing plays a huge role in providing information regarding human genes and chromosomes in many different fields of medicine.
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Causes of osteogenesis imperfecta
Most cases of osteogenesis imperfecta are inherited as autosomal dominant disorders and have a prevalence of 1/20,000. Current genetic analysis techniques are an important foundation for prenatal diagnosis of high-risk subjects with osteogenesis imperfecta in order to prevent and reduce the incidence of the disease.
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Genetic testing before pregnancy
Prenatal genetic testing is used to determine the risk of having a child with a birth defect. Early detection of genetic risks helps parents make informed choices about having children.
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Direction of treatment of types of infertility
Infertility occurs when a couple lives together for a year without using any method of contraception and the wife still cannot get pregnant. This is a fairly common condition, with 10-15% of couples unable to conceive naturally. However, with the development of modern medicine, this problem is no longer a concern if both people agree to visit and receive treatment together.
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Diagnosis of infertility in husband and wife
Pregnancy and childbirth are natural processes that occur in couples who have had sexual activity. However, not all families can achieve complete happiness when they are still haunted by the “disease” of infertility. This is a problem not only caused by the wife but also by the husband or a combination of both. Early recognition and early diagnosis, timely intervention are effective solutions to help quickly receive good news.
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Cardiology Pediatrics Orthopedics