Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A.

Seo, Soo Hyun; Kim, So Yeon; Cho, Sung Im; Park, Hyunwoong; Lee, Seungjun; Choi, Jong Moon; Kim, Man Jin; Lee, Jee Soo; Ahn, Kyung Jin; Song, Mi Kyoung; Bae, Eun Jung; Park, Sung Sup; Seong, Moon Woo

Seo, Soo Hyun; Kim, So Yeon; Cho, Sung Im; Park, Hyunwoong; Lee, Seungjun; Choi, Jong Moon; Kim, Man Jin; Lee, Jee Soo; Ahn, Kyung Jin; Song, Mi Kyoung; Bae, Eun Jung; Park, Sung Sup; Seong, Moon Woo.

Afiliação

Seo SH; Department of Laboratory Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Kim SY; Department of Laboratory Medicine, National Medical Center, Seoul, Korea.
Cho SI; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Park H; Department of Laboratory Medicine, Gyeongsang National University Changwon Hospital, Changwon, Korea.
Lee S; Department of Laboratory Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Choi JM; Green Cross Genome, Yongin, Korea.
Kim MJ; Green Cross Laboratories, Yongin, Korea.
Lee JS; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Ahn KJ; Department of Laboratory Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea.
Song MK; Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.
Bae EJ; Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.
Park SS; Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.
Seong MW; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.

Ann Lab Med ; 38(1): 54-58, 2018 Jan.

Article em En | MEDLINE | ID: mdl-29071820

Assuntos

Canal de Potássio ERG1/genética; Canal de Potássio KCNQ1/genética; Síndrome do QT Longo/diagnóstico; Canal de Sódio Disparado por Voltagem NAV1.5/genética; Aciltransferases; Adolescente; Adulto; Transtorno Autístico/diagnóstico; Transtorno Autístico/genética; Canais de Cálcio Tipo L/genética; Cardiomiopatia Dilatada/diagnóstico; Cardiomiopatia Dilatada/genética; Criança; Pré-Escolar; Eletrocardiografia; Testes Genéticos; Variação Genética; Humanos; Lactente; Síndrome do QT Longo/genética; Polimorfismo de Nucleotídeo Único; Canal de Liberação de Cálcio do Receptor de Rianodina/genética; Sindactilia/diagnóstico; Sindactilia/genética; Taquicardia Ventricular/diagnóstico; Taquicardia Ventricular/genética; Fatores de Transcrição/genética; Adulto Jovem

Palavras-chave

Long QT syndrome; Multigene panel sequencing; Prolonged heart rate-corrected QT interval

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Canal de Potássio KCNQ1 / Canal de Sódio Disparado por Voltagem NAV1.5 / Canal de Potássio ERG1 Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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