Genetic & Reproductive Wellness
Premarital Genetic Screening
Screening for common inherited conditions, including thalassemia, to help couples assess genetic compatibility and reduce the risk of passing on genetic disorders.
Pre-implantation Genetic Diagnosis (PGD) & Screening (PGS)
Used during IVF, PGD and PGS identify embryos with genetic abnormalities, allowing only healthy embryos to be selected for transfer.
Non-Invasive Prenatal Testing (NIPT) – Harmony
A DNA-based blood test for early detection of chromosomal conditions such as Down syndrome—safe for both mother and baby.
Expanded Newborn Screening
Comprehensive screening for conditions that may cause intellectual disabilities, including thalassemia, to enable early intervention.
Future Genetic Risk & Cancer Risk Assessment
Analysis of over 50 cancer-related genes to evaluate inherited risks and support proactive healthcare planning.
Whole Exome Sequencing (WES) & Molecular Diagnosis
Advanced testing using WES technology to detect rare or complex genetic disorders, ideal for individuals with unexplained symptoms.
Cell-Free DNA Testing
A non-invasive method used to detect genetic changes and monitor certain conditions, supporting early and accurate diagnosis.
Paternity Testing & Genetic Identification
DNA testing to determine paternity or individual genetic identity using reliable genome markers.