Accurate Diagnosis of Genetic Conditions
We diagnose conditions caused by abnormalities in genes and chromosomes, working collaboratively with multidisciplinary specialists to deliver precise and individualized care. These include:

• Chromosomal disorders such as Down syndrome, Prader–Willi syndrome, DiGeorge syndrome, Williams syndrome, etc. 
• Single-gene disorders such as thalassemia, hemophilia, muscular dystrophy, inherited metabolic disorders, neurological genetic conditions, and Marfan syndrome 
• Complex diseases with genetic contributions such as cancer, cardiovascular disease, autism, epilepsy, congenital anomalies, and unexplained chronic conditions 
• Rare diseases where the underlying cause remains unknown 

Family Risk Assessment
We provide genetic counseling and risk evaluation for individuals and families with a history of inherited conditions, supporting proactive and informed health management.
Reproductive and Prenatal Planning

• Carrier screening before pregnancy 
• Prenatal genetic diagnosis for fetal abnormalities 
• Counseling on safe and informed reproductive options 

Advanced Therapeutics

• Focus on disease-specific multi-disciplinary care amongst related medical and allied-health specialists
• Medical nutrition therapy for inherited metabolic disorders 
• Enzyme replacement therapy for patients with Gaucher disease and Fabry disease 
• Coordination of referrals to international rare disease support networks and research initiatives, where available

Advanced Genetic Testing Technologies
Our clinic offers state-of-the-art genetic testing, including:

• Whole Genome Sequencing (WGS) 
• Whole Exome Sequencing (WES) 
• Transcriptome Sequencing
• Chromosomal and gene-level analysis throughout lifespan 
• Metabolic Medicine profiles, e.g., plasma amino acid, urine organic acid, and plasma acyl-carnitine
• Genome data and bioinformatic analysis

These technologies enable highly accurate, comprehensive, and timely diagnosis, supporting better clinical outcomes.