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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 1
WARNING: on Feb 2008, we have been aware that this case had simultaneously been published in another Journal (namely Cancer Genet Cytogenet), although double reports are objectionable.
Kavita S. Reddy, Kathy Richkind
 
Clinics
Age and sex : 57 year(s) old female patient.
Previous History : no preleukemia
Organomegaly : no hepatomegaly ; no splenomegaly ; no enlarged lymph nodes ; no central nervous system involvement
Blood
WBC : 3.8 x 109/l; Hb : 11.4 g/dl; platelets : 160 x 109/l;
Cyto pathology classification
Precise diagnosis : Myelodysplastic syndrome (MDS): refractory anaemia
Survival
Treatment : Maintenance therapy for MDS patient declined bone marrow transplantation (BMT)
Relapse : -
Status : Alive
Survival : 42 month(s)
Karyotype
Sample : BM ; culture time : 24/48 h, unstimulated cultures ; banding : G-banding
Results : 46,X,t(X;20)(q13;q13.3)[5]/46,XX[15]
Fig. 1. Partial karyotypes of the translocation t(X;20)(q13;q13.3) for cases 1•4 (top to bottom). Arrows indicate the derivatives 20 and X.
Internal links
Atlas Cardt(X;20)(q13;q13)
Case ReportTranslocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 2
Case ReportTranslocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 3
Case ReportTranslocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 4
Bibliography
Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes.
Michaux L, Wlodarska I, Mecucci C, Hernandez JM, Van Orshoven A, Michaux JL, Van den Berghe H
Cancer genetics and cytogenetics. 1995 ; 82 (1) : 17-22.
PMID 7627929
 
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
 

Contributor(s)
Written01-2005Kavita S. Reddy, Kathy Richkind
Citation
This paper should be referenced as such :
Reddy KS, Richkind KE . Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 1. Atlas Genet Cytogenet Oncol Haematol. January 2005 .
URL : http://AtlasGeneticsOncology.org/Reports/0X20ReddyID100009.html

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indexed on : Mon Aug 11 21:22:54 2008


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