Literature DB >> 16682286

Myelodysplastic syndromes with isolated deletion of the long arm of the chromosome X as a sole cytogenetic change.

Yulia V Olshanskaya1, Alla I Udovichenko, Lubov A Vodinskaya, Eugenia N Glasko, Elena N Parovitchnikova, Yurii Yu Lorie, Valentina N Dvirnik, Valerii G Savchenko, Elena V Domracheva.   

Abstract

Deletions of Xq are extremely rare events in myelodysplastic syndromes (MDS) patients and were previously described in five patients, in two of them as a sole chromosome abnormality. We found isolated del(Xq) in 3 of 127 MDS patients with clonal chromosome changes. Detailed analysis of clinical and morphological data of presented and previously published cases indicates the following: (1) del(X)(q24) and del(X)(q13) are nonrandom chromosomal abnormalities in MDS; (2) MDS with deletions of Xq affect exclusively females ages 46-65; and (3) deletions of Xq are associated with refractory anemia with excess blasts (RAEB) and indicate an unfavorable prognosis.

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Year:  2006        PMID: 16682286     DOI: 10.1016/j.cancergencyto.2005.08.018

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  1 in total

1.  Identification of i(X)(p10) as the sole molecular abnormality in atypical chronic myeloid leukemia evolved into acute myeloid leukemia.

Authors:  Carmelo Gurnari; Paola Panetta; Emiliano Fabiani; Anna Maria Nardone; Diana Postorivo; Giulia Falconi; Luca Franceschini; Manuela Rizzo; Vito Mario Rapisarda; Eleonora De Bellis; Francesco Lo-Coco; Maria Teresa Voso
Journal:  Mol Clin Oncol       Date:  2017-12-29
  1 in total

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