Fluorescence in situ hybridization (FISH) is a cytogenetic technique that uses highly specific fluorescent probes to detect and localize the presence or absence of specific DNA sequences. It is the most convincing technique for locating the specific DNA sequences, diagnosis of genetic diseases, gene mapping, and identification of novel oncogenes or genetic aberrations contributing to various types of cancers.
In the field of conventional and molecular cytogenetics, Suraksha aims to be one stop solution for personalized diagnosis in Eastern India. Here, we strictly adhere to the quality and ethical guidelines and reporting is done as per The International System for Human Cytogenetic Nomenclature (ISCN) Guidelines.
OUR FACILITY:
- Prenatal, Postnatal & Carrier diagnosis - Trisomies (13,18,21), Prader-Willi syndrome, Angelman syndrome, 22q13 deletion syndrome, chromosome abnormalities
- Investigation of Sperm cells quality
- Cancer diagnosis - Chronic myeloid leukemia, Acute lymphoblastic leukemia, Multiple Myeloma
- Targeted therapy for Carcinoma Breast, Carcinoma Stomach, Soft tissue sarcomas etc.
- Monitoring the success of bone marrow transplantation
- Detailed interpretation of report followed by genetic counseling; as supportive aspects only for referring clinicians where ever applicable.
