Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.

Aliazami, Farnoush; Gilani, Sapideh; Farhud, Dariush; Naraghi, Mohsen; Afshari, Mahdi; Eslami, Maryam

Aliazami, Farnoush; Gilani, Sapideh; Farhud, Dariush; Naraghi, Mohsen; Afshari, Mahdi; Eslami, Maryam.

Afiliação

Aliazami F; Department of Genetics, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran; Applied Biotechnology Research Center, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran. Electronic address: farnoush.aliazami@gmail.com.
Gilani S; Department of Surgery, Division of Otolaryngology, University of California, San Diego, 200 West Arbor Drive, MC 8654, San Diego, CA, 92103, United States. Electronic address: sapidehresearch@gmail.com.
Farhud D; School of Public Health, Tehran University of Medical Sciences, Tehran, Iran; Department of Basic Sciences, Iranian Academy of Medical Sciences, Valiasr Sq., 22 Keshavarz Blvd, Tehran, 14, Iran. Electronic address: maryam.eslami2010@gmail.com.
Naraghi M; Department of Otorhinolaryngology-Head and Neck Surgery, TUMS School of Medicine, Rhinology Research Society, Orphans World Wide, 4411 Sunbeam Rd., Jacksonville, FL, 32257, United States. Electronic address: drnaraghi@orphansglobal.org.
Afshari M; Department of Community Medicine, School of Medicine, Zabol University of Medical Sciences, Rajaee Street, Zabol, Iran. Electronic address: mahdiafshari99@gmail.com.
Eslami M; Department of Genetics, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran; Applied Biotechnology Research Center, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran. Electronic address: drmaryam.eslami2020@gmail.com.

Int J Pediatr Otorhinolaryngol ; 168: 111512, 2023 May.

Article em En | MEDLINE | ID: mdl-37086676

Assuntos

Surdez; Perda Auditiva; Humanos; Irã (Geográfico)/epidemiologia; Mutação; Surdez/epidemiologia; Surdez/genética; Perda Auditiva/diagnóstico; Perda Auditiva/epidemiologia; Perda Auditiva/genética; Conexina 26/genética; Conexinas/genética; Proteína 2 com Domínio MARVEL/genética

Palavras-chave

Gene; Hearing loss; Iranian; Non-syndromic; Population; Prevalence; Variant

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Surdez / Perda Auditiva Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies / Systematic_reviews Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2023 Tipo de documento: Article

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