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Rapid Prenatal & Pregnancy Loss
Reproductive Health Tests
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Take the first step toward personalized, non-invasive reproductive health insights.
Rapid Answers for Prenatal Concerns and Pregnancy Loss
Our advanced molecular testing helps identify the genetic causes of pregnancy complications or loss. With rapid turnaround and high accuracy, these tests provide answers during emotionally difficult times—empowering patients and physicians to make informed decisions for future pregnancies.
Conditions Detected by Rapid Prenatal & Pregnancy Loss
01
Chromosomal Abnormalities
02
Miscarriage Causes
03
Fetal Health Complications
04
Maternal-Fetal Genetic Conflicts
Why Early Insight Matters Most
Faster Answers
Get critical genetic results in less time for timely decisions.
Clarity and Closure
Understand the underlying causes of loss to support emotional healing.
Future Preparedness
Helps guide next steps in fertility planning and prenatal care.
Clinically Trusted
Used and recommended by OB-GYNs and fertility specialists worldwide.
How It Works
Quick, Insightful Prenatal Loss Testing Process
Sample Collection
Tissue or blood sample collected post-miscarriage or during prenatal screening.
Genetic Analysis
Sample undergoes rapid chromosomal microarray or sequencing in our certified lab.
Report & Guidance
Receive a detailed genetic report with expert insights and clinical recommendations.
Why Choose FSG?
01
Advanced
Technology
Technology
We use next-generation sequencing for rapid and accurate diagnostic insights.
02
Compassionate Approach
Designed to support emotional and clinical needs during sensitive times.
03
Timely Results
Receive results quickly when decisions and clarity matter most.
04
Trusted Facility
FSG is UAE’s first certified molecular and stem cell lab.
FAQ’s
Frequently Asked Questions!
We’re here to help. Explore answers or reach out to our team directly.
This test is designed to quickly analyze genetic and chromosomal factors related to pregnancy loss or complications, helping identify underlying causes for better medical guidance.
This test is recommended for individuals or couples who have experienced multiple miscarriages, stillbirths, or unexplained pregnancy complications, as well as those undergoing fertility treatments.
The test typically involves a simple blood or tissue sample collection. The sample is then analyzed using advanced genetic sequencing or chromosomal microarray technologies.
Results are usually available within 5 to 10 working days, depending on the lab and complexity of the analysis.
The test provides insight into potential genetic causes of pregnancy loss, enabling personalized care plans, informed future pregnancy planning, and emotional closure.
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