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Blood Cancers

MDRC has complete range of modalities for diagnosis of blood cancer using blood, bone marrow and lymph node samples. Our Haemato-oncology department offers state of art facilities for diagnosing all kinds of Haemato-Lymphoid and Lymphatic disorders . Our reference lab has IVD approved Flow cytometer ( 10 colors and three laser flow cytometer ) for characterization and detection of Minimal Residual Disease (MRD) in Leukemias/Lymphomas.

OurKeyServices

Blood Cancers
  • Bone Marrow Aspirate, Imprints and tissue biopsies with special stains
  • Flow Cytometry
    • Acute Leukemia Basic lineage Panel
    • AML characterization panel
    • ALL Characterization panel
    • Acute Leukemia Comprehensive Diagnostic Panels
    • CLL screening Panel
    • CLL Diagnostic Panel
    • MRD panels
    • Multiple Myeloma Panel
    • MDS panel etc
  • Bone Marrow Karyotyping
  • FISH tests
    • CML (BCR-ABL)
    • CLL (Chr 13q, Trisomy 12, 17p.53, 11q (ATM))
    • AML (AML1-ETO, Trisomy 8, MLL, Inv(16), BCR ABL)
    • MM (Chr 13q, 17p53, 11q(ATM), IgH, FGFR3/IgH)
    • MDS (Del5q, Del 7q) etc
  • Molecular tests
    • JAK2 Gene (V617F) Mutation
    • FLT3 (ITD, D835Y) Mutation
    • BCR-ABL1 Major Quantitative
    • BCR-ABL1 Major, BCR-ABL1 Minor Qualitative
    • BCR-ABL1 Minor Quantitative BCR/ABL Variant Panel (Mbcr-b2a2, b3a2, b2a3, b3a3; mbcr-e1a2, e1a3; µbcr)
    • PML/RARA Qualitative and Quantitative
    • RUNX1-RUNX1T1 (AML1-ETO) t(8;21)
    • CBFB-MYH11 inv(16)
    • TEL/AML1 MLL t(4;11)(q21;q23)
    • E2A t(1;19)(q23;p13)
    • ALL PCR Panel (BCR/ABL t(9;22)(q34;q11), TEL/AML1 t(12;21)(p13;q22), MLL t(4;11)(q21;q23), E2A t(1;19)(q21;q23))
    • Acute Leukemia Mini Panel (AML/ETO, inv(16), PML/RARA, BCR/ABL t(9;22)(q34;q11), TEL/AML1 t(12;21)(p13;q22), MLL t(4;11)(q21;q23), E2A t(1;19)(q21;q23)
    • AML PCR Panel (AML/ETO, inv(16), PML/RARA)
    • BCR/ABL1 Kinase Domain Mutation Myeloproliferative Leukemia Mutation Screening
    • MPL Mutation (MPL - S505N; W515L)
    • JAK 2 Mutation Detection Panel (Exons 12-15)
    • CEBPA Full gene sequencing
    • NPM1 Mutation Analysis (Exon 12 insertion)
    • CALR Mutation Analysis (Deletion or Insertion in Exon 9)
    • Chronic Neutrophilic Leukemia (CNL)(CSF3R Exon 14 & 17; SETBP gene)
    • GATA2 full length gene sequencing
    • c-KIT Mutation Screening (Exons 9, 11, 13, 17) etc.
  • Oncomine Panels
  • USG/CT guided FNAC’s to stage many lymphomas and myelomas
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