CASE REPORTS in
HAEMATOLOGY (Paper co-edited with the European LeukemiaNet) |
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 3 |
Written | 2005-01 | Kavita S Reddy, Kathy Richkind |
Genzyme Genetics, Orange, CA. Kavita.reddy@gmail.com |
Clinics |
Age and sex : | 77 year(s) old female patient. |
Previous History : | no preleukemia |
Organomegaly : no hepatomegaly ; no splenomegaly ; no enlarged lymph nodes ; no central nervous system involvement |
Cyto pathology classification |
Precise diagnosis : Myelodysplastic syndrome (MDS): sideroblastic anemia |
Survival |
Relapse : - |
Status : No clinical information |
Karyotype |
Sample : BM ; culture time : 24/48 h, unstimulated cultures ; banding : G-banding |
Results : 46,X,t(X;20)(q13;q13.3)[10]/46,XX[10] |
![]() |
Fig. 1. Partial karyotypes of the translocation t(X;20)(q13;q13.3) for cases 1ï4 (top to bottom). Arrows indicate the derivatives 20 and X. |
Internal links |
Bibliography |
Biclonal acute monoblastic leukemia showing del(7q) and trisomies 9 and 22. |
Wong KF, Kwong YL, Tang KC |
Cancer genetics and cytogenetics. 1995 ; 82 (1) : 70-72. |
PMID 7627939 |
Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders. |
Gray BA, Cornfield D, Bent-Williams A, Zori RT |
Cancer genetics and cytogenetics. 2003 ; 141 (2) : 169-174. |
PMID 12606138 |
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders. |
Reddy KS, Richkind K, Ross M, Seirra R |
Cancer genetics and cytogenetics. 2005 ; 157 (1) : 70-73. |
PMID 15676151 |
Citation |
This paper should be referenced as such : |
Free journal version : [ pdf ] [ DOI ] |
On line version : http://AtlasGeneticsOncology.org/Reports/0X20ReddyID100011.html |
© Atlas of Genetics and Cytogenetics in Oncology and Haematology | indexed on : Thu Feb 14 18:19:24 CET 2019 |
For comments and suggestions or contributions, please contact us