Literature DB >> 14560778

Cytogenetics of chronic myeloproliferative disorders and related myelodysplastic syndromes.

Adewale Adeyinka1, Gordon W Dewald.   

Abstract

The only MPD associated with any specific chromosome anomaly is CML, which is linked with t(9;22)(q34;q11.2) or a variant of this anomaly. An association exists for del(13)(q12q14) and CIMF; t(5;12)(q33;p13) and CEL; and del(20q11), +8, and +9 and PV, but these anomalies can be seen in various hematologic malignancies. The most common chromosomal anomalies among MPD in order of frequency are t(9;22)(q34;q11.2), -Y, +8, +9, -7, del(20) (q11q13), del(13)(q12q14), del(5)(q13q33), and del(12)(p12). FISH techniques are useful for MPD to study inadequate bone marrow or blood specimens and to monitor disease status among patients with known chromosome anomalies, but they are not more sensitive than conventional chromosome studies.

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Year:  2003        PMID: 14560778     DOI: 10.1016/s0889-8588(03)00087-x

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN: 0889-8588            Impact factor:   3.722


  1 in total

1.  SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD.

Authors:  Lukasz P Gondek; Andrew J Dunbar; Hadrian Szpurka; Michael A McDevitt; Jaroslaw P Maciejewski
Journal:  PLoS One       Date:  2007-11-21       Impact factor: 3.240

  1 in total

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