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Application of fluorescent in situ hybridization in primary diagnosis of aplastic anemia by morphology / 中华医学遗传学杂志
Article em Zh | WPRIM | ID: wpr-287962
Biblioteca responsável: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the clinical application of fluorescent in situ hybridization (FISH) for the differential diagnosis of myelodysplastic syndromes (MDS) and aplastic anemia (AA).</p><p><b>METHODS</b>A FISH kit capable of detecting the chromosomal abnormalities related to MDS was used to analyze 94 patients who were suspected to have AA by bone marrow morphology.</p><p><b>RESULTS</b>Cytogenetic abnormalities were detected in 11 of the 94 patients, which included trisomy 8 (5 cases), 20q- (1 case) and -Y (1 case). There were 4 cases related to MDS, which included 3 cases of 5q-, in which 1 case carry 20q- at the same time, and 7q- (1 case). No significant difference was found between the MDS and AA groups in terms of age, sex or routine blood examination including absolute neutrophil count, hemoglobin content and platelet count.</p><p><b>CONCLUSION</b>FISH can detect certain cytogenetic abnormalities related to MDS in patients morphologically diagnosed as AA.</p>
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Trissomia / Cromossomos Humanos Par 7 / Cromossomos Humanos Par 8 / Células da Medula Óssea / Aberrações Cromossômicas / Hibridização in Situ Fluorescente / Biologia Celular / Diagnóstico / Genética / Anemia Aplástica Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male Idioma: Zh Revista: Chinese Journal of Medical Genetics Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Trissomia / Cromossomos Humanos Par 7 / Cromossomos Humanos Par 8 / Células da Medula Óssea / Aberrações Cromossômicas / Hibridização in Situ Fluorescente / Biologia Celular / Diagnóstico / Genética / Anemia Aplástica Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male Idioma: Zh Revista: Chinese Journal of Medical Genetics Ano de publicação: 2016 Tipo de documento: Article