21/10/2024
Genetic Testing Plays a Vital Role in Diagnosing and Supporting the Treatment of Genetic Disorders. Currently, there are many different genetic testing methods, each serving specific purposes. The specialist doctor will base on the patient’s health condition and needs to recommend the most suitable test.
What is Genetic Testing?
Genetic testing is a process that analyzes changes in the genetics to determine the presence of genetic disorders, classify disease types, or rule out the possibility of disease. Since the genetics is highly complex and genetic changes are diverse, each test only examines one or a few specific types of changes. Therefore, consulting with a genetic specialist is necessary for an accurate test recommendation, helping to identify the genetic cause with the highest effectiveness while optimizing treatment costs.
Purpose of Genetic Testing
Genetic testing is carried out for various purposes, including:
Diagnosing genetic disorders that have manifested in the patient.
Identifying personalized treatment methods to optimize treatment efficacy.
Early detection of genetic disorders before symptoms appear.
Assessing the risk of genetic diseases during the current or future pregnancy.
Planning for the birth of a healthy child in families with known genetic conditions or carriers.
Developing preventive measures for diseases (such as cancer, chronic illnesses) in the future.
Depending on the purpose of the test, the doctor will recommend the appropriate genetic tests. To ensure accuracy and safety, patients should undergo testing at reputable medical institutions with experienced professionals in the field of genetics.
On February 14, 2025, the Andrology and Fertility Hospital of Hanoi had the honor of welcoming the Merck Healthcare delegation. Merck Healthcare is a global leader in the pharmaceutical industry and a long-standing international strategic...
Patau Syndrome is a rare congenital genetic disorder that severely affects the health of the child and can even lead to death either in utero or shortly after birth. Patau Syndrome (or Trisomy 13) is a serious congenital defect caused...
Thalassemia is a hereditary congenital hemolytic anemia caused by the deficiency of one or more globin chains. It is one of the most common genetic disorders worldwide. Currently, it is estimated that about 7% of the global population...
Thalassemia is one of the most common genetic disorders worldwide, affecting future generations. Vietnam is one of the countries with a high prevalence of affected and carrier individuals. The estimated carrier rate is around 2-4%...
On the morning of September 22, 2024, the Andrology and Fertility Hospital of Hanoi (AF HANOI) successfully held the “5th Scientific Conference”. This event was a part of a series of activities in honor of the hospital’s...
With the aim of improving the quality of sexual health care in Vietnam and fostering connections between the scientific communities both domestic and international, the Hanoi Medical University (HMU), Vietnam National University, Hanoi...
This afternoon (September 13), Andrology and Fertility Hospital of Hanoi (AF HANOI) warmly welcomed a delegation of world-renowned experts in gender-affirming surgery and sexual medicine for a visit and collaborative discussions at...
In recent years, infertility has become one of the prominent issues of modern medicine, pressure from work, unscientific lifestyle, along with environmental pollution factors, and mutated genes have been increasing the rate of infertility...
