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  • New Main Page
    ...ollaborative project to document and describe chromosome and other genomic abnormalities in cancer. This resource is supported by the [http://www.cancergenomics.org ...e]] '''Structural Abnormalities''' '''[[:Category:Structural Abnormalities Chromosome 1|1]]'''
    7 KB (905 words) - 22:59, 20 November 2017
  • All Categories
    == Structural == * Structural Abnormalities
    10 KB (1,089 words) - 22:30, 20 November 2017
  • HAEM4Backup:B-Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1
    ...in the production of a ''BCR-ABL1'' fusion, also known as the Philadelphia chromosome (Ph+).   * Philadelphia chromosome
    8 KB (1,060 words) - 12:37, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) Megakaryoblastic with t(1;22)(p13.3;q13.1);RBM15-MKL1
    ...">Arber DA, et al., (2017). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic a ...cal fusions are expressed, the ''RBM15''-''MKL1'' fusion on the derivative chromosome 22 is the candidate oncoprotein because it contains all of the putative fun
    10 KB (1,334 words) - 12:32, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) with t(6;9)(p23;q34.1); DEK-NUP214
    ...">Arber DA, et al., (2017). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic a Accounts for 0.7-1.8% of AML, occurring in both children (median age of 13 years) and adults (median age of 35-44 years)<ref name=":0" />.
    10 KB (1,401 words) - 12:32, 3 November 2023
  • HAEM4Backup:Pure Erythroid Leukemia
    ...(5;12;7)(p15.1;p13;q32),der(7)t(5;12;7),der(12)del(12)p13p13)t(5;12;7),del(13)(q12q14) was reported in a two year old boy with PEL<ref name=":10" />. !Chromosome Number!!Gain/Loss/Amp/LOH!!Region
    15 KB (2,002 words) - 12:34, 3 November 2023
  • HAEM4Backup:Mixed Phenotype Acute Leukemia (MPAL) with t(9;22)(q34.1;q11.2); BCR-ABL1
    ...f>{{Cite journal|last=Manola|first=Kalliopi N.|date=2013|title=Cytogenetic abnormalities in acute leukaemia of ambiguous lineage: an overview|url=https://www.ncbi.n Many cases have other cytogenetic abnormalities in addition to the t(9;22) or a complex karyotype.
    12 KB (1,664 words) - 12:36, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) with t(9;11)(p21.3;q23.3); KMT2A-MLLT3
    ...">Arber DA, et al., (2017). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic a ...st8=Gitte|last9=Andersen|first9=Mette Klarskov|date=2003|title=Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all childr
    12 KB (1,750 words) - 12:32, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) with BCR-ABL1
    ...ion. The t(9:22)(q34.1;q11.2) results in the formation of the Philadelphia chromosome and the chimeric BCR-ABL1 fusion gene. It is worth noting that the fusion g ...there are only a few cases described where acquisition of the Philadelphia chromosome upon disease relapse or transformation of antecedent myelodysplastic syndro
    18 KB (2,578 words) - 12:33, 3 November 2023
  • HAEM4Backup:T-cell lymphoblastic leukemia with t(7;14)(p15;q32)
    ...osomal abnormalities are detected in approximately 50% of T-ALL/LBL. Other abnormalities include cryptic deletions, often of tumor suppressor genes, and other somat Cytogenetic abnormalities of T-ALL/LBL usually involve rearrangements of the T cell receptor (TCR) ge
    7 KB (1,040 words) - 12:57, 3 November 2023
  • HAEM4:T-cell lymphoblastic leukemia with t(7;14)(p15;q32)
    ...osomal abnormalities are detected in approximately 50% of T-ALL/LBL. Other abnormalities include cryptic deletions, often of tumor suppressor genes, and other somat Cytogenetic abnormalities of T-ALL/LBL usually involve rearrangements of the T cell receptor (TCR) ge
    8 KB (1,082 words) - 14:00, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) with t(8;21)(q22;q22.1); RUNX1-RUNX1T1
    ...the leukemia is not classified in the group of AML with recurrent genetic abnormalities due to clinical and prognostic differences. AML with t(8;21)(q22;q22) is a ...s involving chromosomes 8, 21 and a third chromosome occur; the derivative chromosome 8 in the t(8;21)(q22;q22) and the variant t(8;21;var) carries the RUNX1-RUN
    20 KB (2,953 words) - 12:32, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2);GATA2, MECOM
    ...icance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia|url=https://www.ncbi.nlm.nih.gov/pubmed/20660833| #Other 3q abnormalities.
    17 KB (2,499 words) - 12:32, 3 November 2023
  • HAEM4Backup:Acute Myeloid Leukemia (AML) with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11
    ...the leukemia is not classified in the group of AML with recurrent genetic abnormalities due to clinical and prognostic differences. ...distinctive cytogenetic subtype of acute myeloid leukemia. Both of these chromosome rearrangements result in the CBFB-MYH11 gene fusion.
    27 KB (3,873 words) - 12:32, 3 November 2023
  • HAEM4Backup:B-Lymphoblastic Leukemia/Lymphoma, BCR-ABL1-Like
    ...p A.|last9=Bräundl|first9=Kathrin|date=2017|title=Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutati ...et al., (2017). B-lymphoblastic leukaemia/lymphoma with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic a
    19 KB (2,670 words) - 12:38, 3 November 2023
  • BRST5:Phyllodes Tumour
    |Relevant gene: ''EGFR.'' Amplified (and/or with structural rearrangement, most commonly loss of exons 2-7, also known as EGFRvIII) in ...ically relevant gene(s) unknown. Observed in 39-57% of malignant tumors, 7-13% of borderline tumors; not seen in benign tumors <ref name=":6" />.
    16 KB (2,255 words) - 13:27, 29 February 2024
  • HAEM4Backup:B-Lymphoblastic Leukemia/Lymphoma with Hypodiploidy
    ...mphoblastic leukemias. The majority of cases (>80%) fall within the 44-45 chromosome range. However, beyond this, there are three main groups, that although ra ...edscape Article, Drugs & Diseases, Hematology.</ref>. Hypodiploid ALL with chromosome numbers less than 44 is associated with poor prognosis.
    21 KB (2,882 words) - 12:37, 3 November 2023
  • HAEM4:B-Lymphoblastic Leukemia/Lymphoma with Hypodiploidy
    ...mphoblastic leukemias. The majority of cases (>80%) fall within the 44-45 chromosome range. However, beyond this, there are three main groups, that although ra ...edscape Article, Drugs & Diseases, Hematology.</ref>. Hypodiploid ALL with chromosome numbers less than 44 is associated with poor prognosis.
    21 KB (2,915 words) - 13:48, 3 November 2023
  • HAEM4Backup:TEMPI Syndrome
    Somatic Structural variants of translocation: |t(2;13)(2p22.3/q14.2)
    17 KB (2,353 words) - 12:42, 3 November 2023
  • HAEM4:TEMPI Syndrome
    Somatic Structural variants of translocation: |t(2;13)(2p22.3/q14.2)
    17 KB (2,397 words) - 16:35, 4 December 2023

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