Abnormal Mineralization Panel NGS Genetic Test
The Abnormal Mineralization Panel NGS Genetic DNA Test is a diagnostic tool used to identify genetic mutations that may cause abnormal mineralization in bones, teeth, and other tissues. This test is offered by DNA Labs UAE and is designed to provide accurate diagnosis and treatment options for patients with mineralization disorders.
Test Details
The Abnormal Mineralization Panel NGS Genetic DNA Test utilizes next-generation sequencing (NGS) technology to analyze multiple genes associated with mineralization disorders. These disorders include hypophosphatasia, osteogenesis imperfecta, and ectopic calcification.
Components and Pricing
The cost of the Abnormal Mineralization Panel NGS Genetic DNA Test is AED 4400.0. This price includes the analysis of blood samples and the delivery of the test report within 3 to 4 weeks.
Pre-Test Information
Prior to undergoing the Abnormal Mineralization Panel NGS Genetic DNA Test, patients are required to provide their clinical history. Additionally, a genetic counseling session is conducted to create a pedigree chart of family members affected by genetic mutations associated with mineralization disorders. The genes analyzed in this test include ABCC6, ALPL, ANKH, ANO5, AP2S1, BMP1, CA2, CASR, CLCN5, CLCN7, COL1A1, COL1A2, CREB3L1, CRTAP, CYP27B1, CYP2R1, DMP1, ENPP1, FAH, FGF23, FGFR1, FGFR3, FKBP10, GALNT3, GJA1, GNA11, GNAS, GORAB, HPGD, HRAS, IFITM5, KRAS, LRP5, MBTPS2, MTAP, NOTCH2, NRAS, OCRL, OSTM1, P3H1, P4HB, PHEX, PLEKHM1, PLOD2, PLS3, PPIB, PTDSS1, PTH1R, SERPINF1, SERPINH1, SLC26A2, SLC34A1, SLC34A3, SLC9A3R1, SLCO2A1, SNX10, SOST, SOX9, SP7, TBXAS1, TCIRG1, TGFB1, TMEM38B, TNFRSF11A, TNFRSF11B, TNFSF11, TYROBP, VDR, and WNT1.
Benefits of the Test
The results of the Abnormal Mineralization Panel NGS Genetic DNA Test can provide valuable information to healthcare providers. With accurate diagnosis, appropriate treatment options can be determined, and genetic counseling can be offered to patients and their families. This test aids in improving patient outcomes and providing personalized care.
Conclusion
The Abnormal Mineralization Panel NGS Genetic DNA Test offered by DNA Labs UAE is a comprehensive and advanced diagnostic tool for identifying genetic mutations associated with abnormal mineralization. With its use of NGS technology and analysis of multiple genes, this test provides accurate diagnosis and treatment options for patients with mineralization disorders. By undergoing this test, patients can receive personalized care and benefit from genetic counseling sessions. The cost of the test is AED 4400.0, and the test report is delivered within 3 to 4 weeks.
Test Name | Abnormal Mineralization Panel NGS Genetic DNA Test |
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Components | |
Price | 4400.0 AED |
Sample Condition | Blood |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Osteology Dermatology Immunology Disorders |
Doctor | Dermatologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for Abnormal Mineralization Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCC6, ALPL, ANKH, ANO5, AP2S1, BMP1, CA2, CASR, CLCN5, CLCN7, COL1A1, COL1A2, CREB3L1, CRTAP, CYP27B1, CYP2R1, DMP1, ENPP1, FAH, FGF23, FGFR1, FGFR3, FKBP10, GALNT3, GJA1, GNA11, GNAS, GORAB, HPGD, HRAS, IFITM5, KRAS, LRP5, MBTPS2, MTAP, NOTCH2, NRAS, OCRL, OSTM1, P3H1, P4HB, PHEX, PLEKHM1, PLOD2, PLS3, PPIB, PTDSS1, PTH1R, SERPINF1, SERPINH1, SLC26A2, SLC34A1, SLC34A3, SLC9A3R1, SLCO2A1, SNX10, SOST, SOX9, SP7, TBXAS1, TCIRG1, TGFB1, TMEM38B, TNFRSF11A, TNFRSF11B, TNFSF11, TYROBP, VDR, WNT1 |
Test Details | The Abnormal Mineralization Panel NGS Genetic DNA Test is a diagnostic tool used to identify genetic mutations that may cause abnormal mineralization in bones, teeth, and other tissues. This test uses next-generation sequencing (NGS) technology to analyze multiple genes associated with mineralization disorders, such as hypophosphatasia, osteogenesis imperfecta, and ectopic calcification. The results of this test can help healthcare providers make an accurate diagnosis, determine appropriate treatment options, and provide genetic counseling to patients and their families. |