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Clinical and experimental studies on five cases of acute myeloid leukemia with translocation t(16;21)(p11;q22) / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 171-173, 2003.
Article Dans Chinois | WPRIM | ID: wpr-248467
ABSTRACT
<p><b>OBJECTIVE</b>To report five cases of acute myeloid leukemia (AML) with t(16;21)(p11;q22) translocation and the result of chromosome painting analysis on one of them.</p><p><b>METHODS</b>Chromosome specimens were prepared by short-term culture of bone marrow cells. Karyotype analysis was made by R-banding technique. Chromosome painting was performed using whole chromosome probes 16 and 21 in 1 case.</p><p><b>RESULTS</b>Karyotype analysis showed identical translocation t(16;21)(p11;q22) in all five cases, accounting for 0.3% of 1448 cases of acute myeoid leukemia examined in the past fifteen years. Moreover, chromosome painting distinctly demonstrated t(16;21) in one of them. Leukemia blasts did not show hemophagocytosis in all of them.</p><p><b>CONCLUSION</b>t(16;21) translocation is a rare and recurring chromosome rearrangement. It represents a specific type of AML. Chromosome painting technique is a more reliable means for detecting it, compared with the conventional karyotype analysis.</p>
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Translocation génétique / Chromosomes humains de la paire 16 / Chromosomes humains de la paire 21 / Leucémie myéloïde / Cellules cultivées / Maladie aigüe / Hybridation fluorescente in situ / Génétique / Caryotypage Limites du sujet: Adolescent / Adulte / Enfant / Femelle / Humains / Mâle langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2003 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Translocation génétique / Chromosomes humains de la paire 16 / Chromosomes humains de la paire 21 / Leucémie myéloïde / Cellules cultivées / Maladie aigüe / Hybridation fluorescente in situ / Génétique / Caryotypage Limites du sujet: Adolescent / Adulte / Enfant / Femelle / Humains / Mâle langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2003 Type: Article