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Rapid diagnosis of Down's and Edward's syndrome by multiplex real-time quantitative PCR / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 449-452, 2010.
Artigo em Chinês | WPRIM | ID: wpr-234385
ABSTRACT
<p><b>OBJECTIVE</b>To establish a multiplex real-time quantitative PCR method for diagnosis of Down's and Edward's syndrome.</p><p><b>METHODS</b>The sequences of the amyloid precursor protein gene (APP) in the Down's region of chromosome 21 and the thymidylate synthetase gene (TYMS) on chromosome 18 were co-amplified in the same tube. The relative quantitative index DeltaCT value was used to differentiate Down's and Edward's syndrome patient from healthy individual. Four groups of samples, including 36 blood samples from normal controls (group A), 15 amniotic fluid samples from normal pregnancies (group B), 21 samples from patients with Down's syndrome (group C) and 6 samples from patients with Edward's syndrome (group D), were investigated in the study.</p><p><b>RESULTS</b>The mean DeltaCT values of the four groups were -0.48+/-0.15, -0.49+/-0.12, -1.26+/-0.17 and 0.25+/-0.12 respectively. The DeltaCT value from group B was not different from that from group A (P>0.05). However, the DeltaCT values from group C and group D were significantly different from that from group A (P<0.01), and no overlapping was observed.</p><p><b>CONCLUSION</b>The DeltaCT values from multiplex real-time quantitative PCR could be used to rapidly diagnose Down's and Edward's syndrome simultaneously.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Diagnóstico Pré-Natal / Síndrome / Trissomia / Cromossomos Humanos Par 18 / Cromossomos Humanos Par 21 / Reação em Cadeia da Polimerase / Síndrome de Down / Genética / Líquido Amniótico / Métodos Tipo de estudo: Estudo diagnóstico Limite: Feminino / Humanos / Gravidez Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2010 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Diagnóstico Pré-Natal / Síndrome / Trissomia / Cromossomos Humanos Par 18 / Cromossomos Humanos Par 21 / Reação em Cadeia da Polimerase / Síndrome de Down / Genética / Líquido Amniótico / Métodos Tipo de estudo: Estudo diagnóstico Limite: Feminino / Humanos / Gravidez Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2010 Tipo de documento: Artigo