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Take the first step toward personalized, non-invasive reproductive health insights.
Detect Rare Genetic Disorders Early with Advanced Screening
Rare Diseases Screening is designed to detect low-prevalence genetic disorders that often go undiagnosed due to their complexity. Early identification can lead to timely interventions, improved quality of life, and personalized treatment plans. This screening is essential for individuals with unexplained symptoms or a family history of rare conditions.
Conditions Detected by Rare Diseases Screening
01
Neuromuscular Disorders (e.g., SMA, Duchenne Muscular Dystrophy)
02
Metabolic Disorders (e.g., Gaucher, Tay-Sachs, PKU)
03
Genetic Syndromes (e.g., Rett, Noonan, Marfan)
04
Mitochondrial Disorders
Uncover the Unseen, Act with Insight
Early Diagnosis
Identify complex conditions before symptoms progress for better management.
Precision Treatment
Enable targeted therapies based on specific genetic mutations.
Reduce Diagnostic Odyssey
Avoid years of misdiagnosis with a single comprehensive screening. Avoid years of misdiagnosis with a single comprehensive screening.
Family Risk Awareness
Understand hereditary risks to support family planning and preventative care.
How It Works
Smart Screening with Genetic Accuracy
Sample Collection
Blood or saliva sample collected at our facility or sent through home collection kits.
Genomic Analysis
Next-generation sequencing targets hundreds of rare disease genes simultaneously.
Expert Interpretation
Receive a detailed, clinician-reviewed report with medical insights and next steps.
Why Choose FSG for Rare Diseases Screening
01
Cutting-Edge Genomics
We apply high-throughput sequencing for unmatched diagnostic depth.
02
Specialized Team
Geneticists and counselors guide you from results to recommendations.
03
Fast Turnaround
 Results delivered within 10–15 business days for quicker decisions.
04
Trusted Lab Partner
FSG is UAE’s first certified molecular and genomics laboratory.
FAQ’s
Frequently Asked Questions!
We’re here to help. Explore answers or reach out to our team directly.
Infectious disease screening involves a set of medical tests that check for the presence of harmful viruses, bacteria, or other pathogens in the body. These infectious disease screening tests help detect infections early—even before symptoms appear—allowing for timely treatment and reducing the risk of transmission to others.
Infectious disease tests are recommended for people in high-risk groups, including those with several sexual partners, individuals undergoing surgery, pregnant women, organ transplant recipients, or anyone with potential exposure to infections. They’re also useful for routine health checks or before starting certain medications or medical procedures.
Common infectious disease screening tests include screening for HIV, Hepatitis B and C, Syphilis, Cytomegalovirus (CMV), and other viral or bacterial infections. The exact list can vary based on your health history, exposure risks, and the purpose of the screening.
These infectious disease tests typically involve collecting a blood sample or a swab, depending on the type of infection being checked. The sample is analyzed using advanced molecular or serological methods in a certified laboratory for accurate results.
Results for most infectious disease screening tests are usually available within 24 to 72 hours. Some specialized tests may take longer, but you'll typically receive a full report with any necessary follow-up steps soon after the analysis is complete.
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
Personalized Medicine