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Bone Marrow Failure Anemia Panel NGS Genetic Test Cost

Original price was: 6,000 د.إ.Current price is: 4,400 د.إ.

-27%

The “Bone Marrow Failure Anemia Panel NGS (Next-Generation Sequencing) Genetic Test” is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to detect genetic mutations associated with bone marrow failure syndromes. This advanced testing method utilizes next-generation sequencing technology to analyze a broad panel of genes known to be involved in bone marrow failure, helping to identify the genetic underpinnings of anemia and related conditions. With a cost of 4400 AED, this test provides invaluable insights for the accurate diagnosis and tailored treatment of patients suffering from bone marrow failure anemias, guiding healthcare professionals in making informed decisions regarding patient care.

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Bone Marrow Failure Anemia Panel NGS Genetic Test

Test Name: Bone marrow failure Anemia panel NGS Genetic DNA Test

Components Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Hematology

Doctor: Hematologist

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for Bone marrow failure Anemia panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCB7, ACTN1, ADAMTS13, AK2, ALAS2, AMN, ANK1, ANKRD26, AP3B1, ATM, ATRX, BLM, BLOC1S3, BRCA1, BRCA2, BRIP1, C15orf41, CASP10, CBL, CBLIF, CD36, CD40LG, CDAN1, CENPJ, CEP152, CLCN7, CLPB, CSF3R, CTC1, CUBN, CXCR4, CYB5R3, CYCS, DHFR, DIAPH1, DKC1, DTNBP1, ELANE, EPB42, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FAS, FASLG, G6PC3, G6PD, GATA1, GFI1, GFI1B, GLRX5, GNE, GP1BA, GP1BB, GP9, GPI, GSS, HAX1, HBA1, HBA2, HBB, HFE, HOXA11, HPS1, HPS3, HPS4, HPS5, HPS6, HSPA9, IL2RG, ITGA2B, ITGB3, ITK, JAGN1, KLF1, KRAS, LIG4, LPIN2, LYST, MLH1, MPL, MRE11, MSH2, MSH6, MTR, MTRR, MYH9, NBN, NF1, NHP2, NOP10, NRAS, PALB2, PARN, PC, PDHA1, PDHX, PKLR, PMS2, PRF1, PTPN11, PUS1, RAC2, RAD51C, RBBP8, RBM8A, RIT1, RPL11, RPL15, RPL26, RPL27, RPL35A, RPL5, RPS10, RPS17, RPS19, RPS24, RPS26, RPS27, RPS28, RPS29, RPS7, RTEL1, RUNX1, SAMD9, SBDS, SEC23B, SH2D1A, SLC19A2, SLC19A3, SLC25A19, SLC25A38, SLC4A1, SLX4, SPTA1, SPTB, SRP72, STIM1, STX11, STXBP2, TCN2, TERT, TINF2, TP53, TPK1, TRNT1, UBE2T, UNC13D, VPS13B, VPS45, WAS, WRAP53, XIAP, XRCC2, YARS2

Test Details

Bone marrow failure anemia panel NGS genetic DNA test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze multiple genes associated with bone marrow failure syndromes and anemia. This test can identify genetic mutations that cause bone marrow failure and anemia, which can help diagnose the condition and guide treatment decisions. The panel includes genes such as GATA1, MPL, RUNX1, and others. This test can be helpful for patients with unexplained anemia, thrombocytopenia, or other blood disorders, and for those with a family history of bone marrow failure syndromes. The results of this test can provide valuable information for the management and treatment of bone marrow failure and anemia.

 

Test Name Bone marrow failure Anemia panel NGS Genetic DNA Test
Components  
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for Bone marrow failure Anemia panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCB7, ACTN1, ADAMTS13, AK2, ALAS2, AMN, ANK1, ANKRD26, AP3B1, ATM, ATRX, BLM, BLOC1S3, BRCA1, BRCA2, BRIP1, C15orf41, CASP10, CBL, CBLIF, CD36, CD40LG, CDAN1, CENPJ, CEP152, CLCN7, CLPB, CSF3R, CTC1, CUBN, CXCR4, CYB5R3, CYCS, DHFR, DIAPH1, DKC1, DTNBP1, ELANE, EPB42, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FAS, FASLG, G6PC3, G6PD, GATA1, GFI1, GFI1B, GLRX5, GNE, GP1BA, GP1BB, GP9, GPI, GSS, HAX1, HBA1, HBA2, HBB, HFE, HOXA11, HPS1, HPS3, HPS4, HPS5, HPS6, HSPA9, IL2RG, ITGA2B, ITGB3, ITK, JAGN1, KLF1, KRAS, LIG4, LPIN2, LYST, MLH1, MPL, MRE11, MSH2, MSH6, MTR, MTRR, MYH9, NBN, NF1, NHP2, NOP10, NRAS, PALB2, PARN, PC, PDHA1, PDHX, PKLR, PMS2, PRF1, PTPN11, PUS1, RAC2, RAD51C, RBBP8, RBM8A, RIT1, RPL11, RPL15, RPL26, RPL27, RPL35A, RPL5, RPS10, RPS17, RPS19, RPS24, RPS26, RPS27, RPS28, RPS29, RPS7, RTEL1, RUNX1, SAMD9, SBDS, SEC23B, SH2D1A, SLC19A2, SLC19A3, SLC25A19, SLC25A38, SLC4A1, SLX4, SPTA1, SPTB, SRP72, STIM1, STX11, STXBP2, TCN2, TERT, TINF2, TP53, TPK1, TRNT1, UBE2T, UNC13D, VPS13B, VPS45, WAS, WRAP53, XIAP, XRCC2, YARS2
Test Details Bone marrow failure anemia panel NGS genetic DNA test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze multiple genes associated with bone marrow failure syndromes and anemia. This test can identify genetic mutations that cause bone marrow failure and anemia, which can help diagnose the condition and guide treatment decisions. The panel includes genes such as GATA1, MPL, RUNX1, and others. This test can be helpful for patients with unexplained anemia, thrombocytopenia, or other blood disorders, and for those with a family history of bone marrow failure syndromes. The results of this test can provide valuable information for the management and treatment of bone marrow failure and anemia.
SKU: TEST-869 Category:

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