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Take the first step toward personalized, non-invasive reproductive health insights.
Know Your Genetic Risks Before Planning a Family
Carrier Screening is a genetic test used to determine whether an individual carries a gene for certain inherited conditions, even if they show no symptoms. This test is essential for individuals or couples planning a family, helping to assess the risk of passing genetic disorders to their children.
Conditions Detected by Carrier Screening
01
Cystic Fibrosis
02
Spinal Muscular Atrophy (SMA)
03
Tay-Sachs Disease
04
Sickle Cell Anemia and other hemoglobinopathies
Empowering Family Planning with Genetic Insight
Early Risk Awareness
Identify your risk of passing on inherited conditions before pregnancy.
Informed Reproductive Choices
Make confident decisions with a clearer understanding of genetic risks.
Partner Compatibility
Understand shared risks between partners for inherited disorders.
Peace of Mind
Reduce uncertainty with reliable insights into your carrier status.
How It Works
Simple Steps to Smarter Parenthood
Sample Collection
A quick blood or saliva sample is collected at our lab or via home kit.
Genetic Screening
Your DNA is analyzed for carrier status of multiple inherited conditions.
Report &Consultation
Receive a comprehensive report with expert consultation for next-step guidance.
Why Choose FSG for Carrier Screening
01
Comprehensive Panels
We screen for 400+ genetic conditions using validated testing methods.
02
Genetic Counseling
Access to board-certified counselors for personalized guidance and support.
03
Fast & Accurate Results
 Get reliable results in a few business days with high accuracy.Â
04
Accredited Lab
FSG is the UAE’s first certified molecular stem cell and genomics facility.
FAQ’s
Frequently Asked Questions!
We’re here to help. Explore answers or reach out to our team directly.
Carrier Screening is a genetic test that identifies whether you carry a gene for certain inherited conditions. It helps determine the risk of passing these conditions to your children.
Anyone planning to start a family can benefit from carrier screening, especially if there's a family history of genetic disorders or if you're part of an ethnic group with a higher risk for certain conditions.
It screens for a wide range of inherited disorders, including cystic fibrosis, spinal muscular atrophy, thalassemia, Tay-Sachs disease, and many more, depending on the panel chosen.
The test is simple and non-invasive. It requires a blood or saliva sample, which is then analyzed in a lab to detect specific genetic mutations.
If you're a carrier, genetic counseling is recommended. Your partner may also be tested, and together, you'll receive guidance on reproductive options to help make informed decisions.
Non-Invasive Prenatal Testing/Screening
Pre-Implantation Genetic Testing/Screening (PGT/PGS)
Male/Female Fertility
Rapid Prenatal & Pregnancy Loss
Maternal Cell Contamination (MCC)
Product of Conception (POC)
My HLA (Human Leucocyte Antigen)
Whole Genome Sequencing (WGS)
Whole Exome Sequencing (WES)
Low Pass Sequencing (1-3x Coverage)
Comprehensive Oncology Screening
Breast Cancer Screening (BRCA)
Cervical Cancer Screening
Prostate Cancer Screening
Heredity Cancer Panel
Leukemia Panel
Lymphoma Panel
Carrier Screening
Newborn Screening
Infectious Diseases Screening
Rare Diseases Screening
Consumer Genomics
Gut Metagenomics
Metagenomics
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