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Application of multiple MLL gene rearrangement detection techniques for children with acute mononuclear leukemia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 1077-1080, 2019.
Article Dans Chinois | WPRIM | ID: wpr-776743
ABSTRACT
OBJECTIVE@#To assess the value of detecting multiple rearrangements of MLL gene in children with acute mononuclear leukemia (AML).@*METHODS@#Eighty six children with AML were analyzed by fluorescence in situ hybridization (FISH), chromosomal karyotyping and multiplex reverse transcription-PCR (RT-PCR).@*RESULTS@#Cross signals were detected by FISH in 26 cases, and 30.2% were detected with MLL gene rearrangements. R-band karyotyping analysis revealed 14 translocations with breakages involving 11q23 and 5 other aberrations, which yielded an overall detection rate of 22.1%. Multiple RT-PCR has detected 12 fusion genes produced by the MLL translocation, which yielded a detection rate of 14.0%. A significant difference was found in the detection rate of the three methods (P< 0.05).@*CONCLUSION@#Combined use of FISH, chromosomal karyotyping and multiplex RT-PCR can improve the detection of MLL gene rearrangements and provide important clues for clinical diagnosis, treatment and prognosis of AML.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Translocation génétique / Chromosomes humains de la paire 11 / Réarrangement des gènes / Leucémie aigüe myéloïde / Histone-lysine N-methyltransferase / Hybridation fluorescente in situ / Protéine de la leucémie myéloïde-lymphoïde / Génétique / Caryotypage Type d'étude: Etude diagnostique Limites du sujet: Enfant / Humains langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2019 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Translocation génétique / Chromosomes humains de la paire 11 / Réarrangement des gènes / Leucémie aigüe myéloïde / Histone-lysine N-methyltransferase / Hybridation fluorescente in situ / Protéine de la leucémie myéloïde-lymphoïde / Génétique / Caryotypage Type d'étude: Etude diagnostique Limites du sujet: Enfant / Humains langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2019 Type: Article