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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.
Artigo em Chinês | 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.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Translocação Genética / Cromossomos Humanos Par 11 / Rearranjo Gênico / Leucemia Mieloide Aguda / Histona-Lisina N-Metiltransferase / Hibridização in Situ Fluorescente / Proteína de Leucina Linfoide-Mieloide / Genética / Cariotipagem Tipo de estudo: Estudo diagnóstico Limite: Criança / Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2019 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Translocação Genética / Cromossomos Humanos Par 11 / Rearranjo Gênico / Leucemia Mieloide Aguda / Histona-Lisina N-Metiltransferase / Hibridização in Situ Fluorescente / Proteína de Leucina Linfoide-Mieloide / Genética / Cariotipagem Tipo de estudo: Estudo diagnóstico Limite: Criança / Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2019 Tipo de documento: Artigo