The Clinical Cytogenetics Department at our lab specializes in the study of chromosomal abnormalities and their impact on human health. Using cutting-edge genetic testing methods, our skilled geneticists and technologists examine patient samples to identify and characterize chromosomal alterations. These findings are crucial for diagnosing genetic disorders, birth defects, and certain types of cancer. Clinicians can confidently refer their patients to us for comprehensive cytogenetic analyses, enabling them to provide personalized and effective medical management. Department in our lab is dedicated to providing a wide range of services to support patients and clinicians in their healthcare journey. Through advanced technologies and the expertise of our professionals, we strive to offer accurate and comprehensive diagnostic solutions for better patient outcomes.
Our Key Services
- Karyotyping to detect chromosomal abnormalities
- Fluorescence In Situ Hybridization (FISH) for targeted genetic investigations
- Array Comparative Genomic Hybridization (aCGH) for comprehensive genomic profiling
- Prenatal diagnostic tests- such as chorionic villus sampling and amniocentesis for fetal chromosomal abnormalities. if a prenatal screening test indicates a possible problem or age, family history or medical history indicates an increased risk of having a baby with a genetic problem.