Down Syndrome is a genetic disorder caused by the presence of an extra copy of chromosome 21. It affects about 1 in every 700 babies born and is associated with developmental delays, physical growth challenges, and distinctive facial features.
Understanding Down Syndrome and the available testing options is crucial for expectant parents. Early testing and diagnosis provide vital information for managing the health and development of the child.
Our center mainly provides services in the fields of genetic counseling, cytogenetics, molecular cytogenetics and molecular genetics. The problems of our patients who apply to our center, which are thought to have genetic causes, are helped by using up-to-date information and technology.
Chromosome disorders form an important category of genetic disease. Cytogenetic tests examine the number and morphology of chromosomes.
Diseases that cause deterioration of human health and change the living order are diagnosed and detected through molecular tests.
It is a discipline that expands the scope and increases the diagnostic value of routine chromosome analysis with the combined use of molecular biology and cytogenetic techniques.
Diagnosis of cancer at an early stage greatly affects the success of cancer treatment. Many cancer tests are performed in our genetic diagnosis center.
We offer genetic analysis and clinical consultancy services at the highest technology and quality standards, using the most up-to-date scientific knowledge, diagnosis and treatment methods.