Genetic Laboratory

GENETIC LABORATORY – WHAT IS IT?

Our genetics laboratory is structured to perform advanced molecular analyses that play a critical role in hereditary diseases, individual genetic predispositions, cancer genetics, and personalized treatment approaches. A wide variety of tests is offered using NGS (Next-Generation Sequencing), PCR, qPCR, and microdeletion/duplication techniques.

Genetic tests guide early diagnosis, treatment selection, and family planning. Our laboratory provides services with an expert team in both clinical and molecular genetics.

WHEN IS IT USED?

Genetic laboratory tests are used for diagnosing hereditary diseases, determining cancer risk, selecting appropriate treatments, family planning, and understanding individual genetic predispositions. These tests are essential for personalized medicine approaches and early intervention strategies.

SOME OF THE MAIN TESTS PERFORMED:

• Comprehensive NGS panels: Oncogenetic, cardiogenetic, and metabolic disease panels
• Carrier screening tests: SMA, cystic fibrosis, thalassemia, etc.
• Prenatal genetic analyses: Non-invasive prenatal tests (NIPT), PGT support processes
• Chromosome analyses: Karyotype, FISH examinations
• Pharmacogenetic tests: Drug sensitivity and metabolism profiling
• Thrombophilia panel: Leiden mutation, prothrombin mutation, etc.
• Microdeletion–duplication screenings: Detection of chromosomal microdeletions and duplications
• Cancer genetics: BRCA1/BRCA2, Lynch syndrome, familial cancer panel
• Neurological genetics: Epilepsy, neurodegenerative disease panels
• Cardiovascular genetics: Familial hypercholesterolemia, cardiomyopathy panels

ADVANTAGES

• Advanced NGS technology
• Expert clinical and molecular genetics team
• Comprehensive test panels
• Personalized medicine approach
• Early diagnosis and intervention
• Family planning guidance