Department of Genetics Laboratory

The Nasl-e Omid Genetics Department, composed of genetic counselors and a genetic laboratory, identifies existing genetic issues within the family by reviewing family history, creating family pedigrees, conducting specialized genetic tests, and analyzing the results. They provide diagnostic and treatment methods before and during pregnancy.

Additionally, even if no genetic problems are found in the family, it is recommended that counseling sessions continue throughout the pregnancy. This is because any small defect during pregnancy can pose risks to the health of both the mother and the fetus.

All the traits that an individual inherits from their parents, such as height, intelligence, eye color, metabolism, and diseases, are passed down through units called genes. These genes are located on structures called chromosomes, which are situated in the nucleus of cells. Humans have 23 pairs of chromosomes (46 in total), with one chromosome from each pair inherited from the father and the other from the mother. Additionally, it has been discovered that the cause of certain genetic diseases is due to abnormalities in the chromosomes. This can involve an increase or decrease in the number of chromosomes or structural changes, which result in the development of disease. Identifying the status of chromosomes and analyzing their numerical or structural changes can be done through cytogenetic methods and a karyotype.

Genetic counseling before and during pregnancy is one of the most critical periods for ensuring a healthy pregnancy. With the help of ultrasound, screening tests, and genetic tests, you can become aware of the developing fetus’s progress and identify issues such as common chromosomal abnormalities, developmental anomalies, or other conditions that might threaten the health of both the mother and the child.

During this time, Nasl-e Omid Clinic strives, with the help of specialized counselors, to identify potential problems and manage them effectively.

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