Showing 17–32 of 67 results
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Fragile X (FMR1) Mutation Screen (L)
3.400,00 د.إThe Fragile X (FMR1) Mutation Screen (L) is a genetic test designed to detect mutations in the FMR1 gene, which are associated with Fragile X syndrome, a leading cause of inherited intellectual disability and autism. This screening identifies CGG repeat expansions, distinguishing between normal, premutation, and full mutation alleles. Key benefits include early detection for informed reproductive decisions, risk assessment for carriers, and guidance for personalized medical management. Utilizing advanced molecular techniques, the test ensures high accuracy and reliability. Ideal for individuals with a family history of Fragile X or unexplained developmental delays, this screening provides critical genetic insights for proactive healthcare planning.
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Sale!
Gut Microbiome Test
Original price was: 4.750,00 د.إ.2.800,00 د.إCurrent price is: 2.800,00 د.إ.Unlock your gut’s potential with our Advanced Gut Microbiome Test . Get a personalized roadmap to optimize digestion, immunity, and overall wellness through cutting-edge microbial analysis and tailored recommendations. Easy, at-home testing with science-backed results.
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HER-2/NEU – FISH Test
2.820,00 د.إThe HER-2/NEU – FISH Test is a highly precise diagnostic tool used to detect HER-2 gene amplification in breast cancer and other malignancies. Utilizing Fluorescence In Situ Hybridization (FISH) technology, it provides accurate, reliable, and early detection of HER-2 status, which is crucial for determining targeted therapy eligibility, such as Herceptin (trastuzumab) treatment.
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Hereditary Cancer Gene Panel – 57 ACMG Genes for Genetic Risk Screening
4.000,00 د.إThe **Hereditary Cancer Gene Panel (57 ACMG Genes)** is a comprehensive genetic test designed to assess inherited cancer risk by analyzing 57 clinically significant genes recommended by the **American College of Medical Genetics (ACMG)**. This panel identifies mutations linked to various hereditary cancers, including **breast, ovarian, colorectal, prostate, and pancreatic cancers**, enabling early detection and personalized risk management. Key features include **next-generation sequencing (NGS) technology** for high accuracy, expert-reviewed results, and actionable insights for **preventive care and targeted treatment strategies**. Ideal for individuals with a family history of cancer, this test empowers proactive healthcare decisions, offering **lifelong benefits through early intervention and precision medicine**.
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Hereditary Cancer Panel 57 ACMG 20 HBOC & 865 literature reviewed Genes
4.000,00 د.إThe **Hereditary Cancer Panel 57 ACMG 20 HBOC & 865 Literature-Reviewed Genes** is a comprehensive genetic test designed to assess hereditary cancer risk. It analyzes **57 key genes**, including the **ACMG 20** and **HBOC-related genes**, alongside **865 literature-reviewed genes**, ensuring a thorough evaluation of cancer predisposition. This panel covers a wide range of hereditary cancers, including **breast, ovarian, colorectal, and more**, providing **clinically actionable insights** for early detection and personalized risk management. Utilizing **advanced sequencing technology**, it delivers **high accuracy and reliability**, making it an essential tool for **patients, healthcare providers, and genetic counselors**. Its unique combination of **expert-curated genes and extensive literature review** enhances diagnostic precision, setting it apart as a **cutting-edge solution for hereditary cancer risk assessment**.
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HIGH RESOLUTION-HLA A B C DR DQ DP TYPING
4.200,00 د.إHIGH RESOLUTION-HLA A B C DR DQ DP TYPING is an advanced genetic test that provides precise, high-resolution typing of HLA Class I (A, B, C) and Class II (DR, DQ, DP) genes. It offers unparalleled accuracy in identifying HLA alleles, making it essential for organ and stem cell transplantation, disease association studies, and immunological research. Utilizing cutting-edge sequencing technology, this test ensures detailed allele-level resolution, improving donor-recipient matching and reducing transplant rejection risks. Its comprehensive coverage and high sensitivity make it a critical tool for personalized medicine, autoimmune disease research, and pharmacogenomics.
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Jak 2 Exon 12-15 Mutation Analysis | Accurate Genetic Testing & Results
2.720,00 د.إThe Jak 2 Exon 12-15 Mutation Analysis is a specialized genetic test designed to detect mutations in exons 12-15 of the JAK2 gene, which are associated with myeloproliferative neoplasms (MPNs) such as polycythemia vera (PV) and other hematologic disorders. This test offers high sensitivity and specificity, enabling early and accurate diagnosis, which is crucial for targeted treatment decisions and disease monitoring. Unlike standard JAK2 V617F mutation tests, this analysis identifies rare but clinically significant mutations, providing comprehensive genetic profiling for patients with suspected MPNs. Its advanced molecular technology ensures reliable results, supporting personalized therapeutic strategies and improving patient outcomes.
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Karyotyping – Products Of Conception (L)
2.400,00 د.إUnlock critical genetic insights with **Karyotyping – Products of Conception (L)**, a specialized diagnostic test designed to analyze chromosomal abnormalities in fetal tissue following pregnancy loss. This advanced cytogenetic analysis provides essential information to help identify potential genetic causes of miscarriage, offering valuable guidance for future reproductive planning.
