Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing loss.

Wu, Lihua; Liu, Yunliang; Wu, Jianman; Chen, Sheng; Tang, Shupin; Jiang, Yi; Dai, Pu

Wu, Lihua; Liu, Yunliang; Wu, Jianman; Chen, Sheng; Tang, Shupin; Jiang, Yi; Dai, Pu.

Afiliação

Wu L; Department of Otolaryngology, Head and Neck Surgery, Nanfang Hospital, Southern Medical Uiversity, Guangzhou, Guangdong, P.R. China.
Liu Y; Department of Otolaryngology, Head and Neck Surgery, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou 350001, Fujian, P.R. China.
Wu J; Department of Otolaryngology, Fujian Provincial Maternity and Children Hospital, Fuzhou 350001, Fujian, P.R. China.
Chen S; Department of Radiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou 350001, Fujian, P.R. China.
Tang S; Department of Ultrasound, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou 350001, Fujian, P.R. China.
Jiang Y; Department of Otolaryngology, Head and Neck Surgery, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou 350001, Fujian, P.R. China.
Dai P; Department of Otolaryngology, Head and Neck Surgery, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou 350001, Fujian, P.R. China dr.jiangyi@163.com daipu301@vip.sina.com.

Biosci Rep ; 39(3)2019 03 29.

Article em En | MEDLINE | ID: mdl-30842343

Assuntos

Orelha Interna/metabolismo; Perda Auditiva Neurossensorial/genética; Mutação; Transportadores de Sulfato/genética; Osso Temporal/metabolismo; Aqueduto Vestibular/anormalidades; Adolescente; Alelos; Criança; Análise Mutacional de DNA; Orelha Interna/diagnóstico por imagem; Orelha Interna/patologia; Feminino; Genótipo; Perda Auditiva Neurossensorial/diagnóstico; Humanos; Masculino; Fenótipo; Osso Temporal/diagnóstico por imagem; Osso Temporal/patologia; Tomografia Computadorizada por Raios X/métodos; Tri-Iodotironina/metabolismo; Adulto Jovem

Palavras-chave

CT phenotype; SLC26A4 gene mutation; Sensorineural hearing loss

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osso Temporal / Aqueduto Vestibular / Transportadores de Sulfato / Perda Auditiva Neurossensorial / Orelha Interna / Mutação Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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