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1.
Acta Academiae Medicinae Sinicae ; (6): 289-294, 2005.
Artículo en Chino | WPRIM | ID: wpr-343720

RESUMEN

<p><b>OBJECTIVE</b>To investigate the molecular pathology in families with long QT syndrome (LQTS) including Jervell-Longe-Nielsen syndrome (JLNS) and Romano-ward syndrome (RWS) and Brugada syndrome (BS) in Chinese population.</p><p><b>METHODS</b>Polymerase chain reaction and DNA sequencing were used to screen for KCNQ1, KCNH2, KCNE1, and SCN5A mutation.</p><p><b>RESULTS</b>We identified a novel mutation N1774S in the SCN5A gene of the BS family, a novel mutation G314S in a RWS family which had also been found in Europe, North America, and Japan, and a single nucleotide polymorphisms (SNPs) G643S in the KCNQ1 of the JLNS family. In this JLNS family, another heterozygous novel mutation in exon 2a was found in KCNQ1 of the patients.</p><p><b>CONCLUSION</b>New mutations were found in our experiment, which expand the spectrum of KCNQ1 and SCN5A mutations that cause LQTS and BS.</p>


Asunto(s)
Adolescente , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Secuencia de Bases , Canal de Potasio ERG1 , Canales de Potasio Éter-A-Go-Go , Genética , Síndrome de Jervell-Lange Nielsen , Genética , Canal de Potasio KCNQ1 , Genética , Síndrome de QT Prolongado , Genética , Datos de Secuencia Molecular , Proteínas Musculares , Genética , Mutación , Linaje , Canales de Potasio con Entrada de Voltaje , Genética , Síndrome de Romano-Ward , Genética , Canales de Sodio , Genética
2.
Chinese Journal of Medical Genetics ; (6): 68-70, 2005.
Artículo en Chino | WPRIM | ID: wpr-321157

RESUMEN

<p><b>OBJECTIVE</b>To identify the mutation of a Chinese family with inherited long QT syndrome(LQTS).</p><p><b>METHODS</b>The disease-causing gene was tentatively determined in light of the clinical manifestations and electrophysiological properties, and then polymerase chain reaction and DNA sequencing were used for screening and identifying mutation.</p><p><b>RESULTS</b>A missense mutation G940A(G314S) in the KCNQ1 gene was identified, which was the 'hot spot' of long QT syndrome mutation.</p><p><b>CONCLUSION</b>The mutation that is involved with long QT syndrome in Chinese patients is the same as that in the European, American and Japanese patients.</p>


Asunto(s)
Femenino , Humanos , Masculino , China , Análisis Mutacional de ADN , Salud de la Familia , Predisposición Genética a la Enfermedad , Genética , Genotipo , Canal de Potasio KCNQ1 , Genética , Síndrome de QT Prolongado , Diagnóstico , Genética , Mutación Missense , Linaje , Reacción en Cadena de la Polimerasa
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