Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysis.

Chen, Anhai; Song, Jian; Acke, Frederic R E; Mei, Lingyun; Cai, Xinzhang; Feng, Yong; He, Chufeng

Chen, Anhai; Song, Jian; Acke, Frederic R E; Mei, Lingyun; Cai, Xinzhang; Feng, Yong; He, Chufeng.

Afiliación

Chen A; Department of Otorhinolaryngology, Xiangya Hospital Central South University, Changsha, Hunan, China.
Song J; Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, Hunan, China.
Acke FRE; National Clinical Research Centre for Geriatric Disorders, Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Mei L; Department of Otorhinolaryngology, Xiangya Hospital Central South University, Changsha, Hunan, China.
Cai X; Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, Hunan, China.
Feng Y; National Clinical Research Centre for Geriatric Disorders, Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.
He C; Department of Otorhinolaryngology, Ghent University/Ghent University Hospital, Ghent, Belgium.

Clin Genet ; 100(1): 3-13, 2021 07.

Article en En | MEDLINE | ID: mdl-33624842

Asunto(s)

Síndrome Branquio Oto Renal/genética; Enfermedades del Oído/genética; Animales; Genotipo; Humanos; Mutación/genética; Fenotipo

Palabras clave

branchial-oto-renal syndrome; branchio-otic syndrome; branchiootorenal spectrum disorder; genotype; hearing loss; phenotype

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome Branquio Oto Renal / Enfermedades del Oído Tipo de estudio: Systematic_reviews Límite: Animals / Humans Idioma: En Revista: Clin Genet Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google