Tripathi P, Deshmukh P (2022) Sudden sensorineural hearing loss: a review. Cureus. https://doi.org/10.7759/cureus.29458
Article PubMed PubMed Central Google Scholar
Lanzieri TM, Chung W, Flores M, Blum P, Caviness AC, Bialek SR et al (2017) Hearing loss in children with asymptomatic congenital cytomegalovirus infection. Pediatrics. https://doi.org/10.1542/peds.2016-2610
Article PubMed PubMed Central Google Scholar
Traylor K, Dodson S, Kralik S, Ho C, Radhakrishnan R (2019) Inner ear anomalies in congenital hearing loss: imaging, genetics, and associated syndromes. Neurographics 9(6):358–372
Wei C-C, Razzak AA, Ghasemi H, Khedri R, Fraase A (2024) Ca2+ binding shifts dimeric dual oxidase’s truncated EF-hand domain to monomer. Biophys Chem 312:107271
Article CAS PubMed Google Scholar
van Beeck CE, Engel M, van de Kamp J, Yntema H, Goverts S, Mulder M et al (2019) The etiological evaluation of sensorineural hearing loss in children. Eur J Pediatr 178(8):1195–1205
Zhou Y, Li C, Li M, Zhao Z, Tian S, Xia H et al (2019) Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province. Mol Genet Genomic Med 7(3):e537
Article PubMed PubMed Central Google Scholar
Alimardani M, Hosseini SM, Khaniani MS, Haghi MR, Eslahi A, Farjami M et al (2019) Targeted mutation analysis of the SLC26A4, MYO6, PJVK and CDH23 genes in Iranian patients with AR nonsyndromic hearing loss. Fetal Pediatr Pathol 38(2):93–102
Article CAS PubMed Google Scholar
de Guimaraes TAC, Arram E, Shakarchi AF, Georgiou M, Michaelides M (2023) Inherited causes of combined vision and hearing loss: clinical features and molecular genetics. Br J Ophthalmol 107(10):1403–1414
Davoudi-Dehaghani E, Bagherian H, DabbaghBagheri S, Mahdieh N, Shirkavand A, Zeinali S (2016) Homozygosity mapping and CDH23 mutation analysis in Iranian deaf families. Hear Balance Commun 14(4):189–193
Dai Z-Y, Sun B-C, Huang S-S, Yuan Y-Y, Zhu Y-H, Su Y et al (2015) Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China. Gene 570(2):272–276
Article CAS PubMed Google Scholar
Tabatabaiefar MA, Montazer Zohouri M, Shariati L, Safari Chaleshtori J, Ashrafi K, Gholami A et al (2010) Mutation analysis of GJB2 and GJB6 genes and the genetic linkage analysis of five common DFNB loci in the Iranian families with autosomal recessive non-syndrom. J Sci Islam Republic Iran. 21(2):2
Alipour H, Saudi A, Mirazi H, Kazemi MH, Alavi O, Zeraatpisheh Z et al (2022) The effect of vitamin C-loaded electrospun polycaprolactone/poly (Glycerol Sebacate) fibers for peripheral nerve tissue engineering. J Polym Environ 30(11):4763–4773
Azadegan-Dehkordi F, Bahrami T, Shirzad M, Karbasi G, Yazdanpanahi N, Farrokhi E et al (2019) Mutations in GJB2 as major causes of autosomal recessive non-syndromic hearing loss: first report of c. 299–300delAT mutation in Kurdish population of Iran. J Audiol Otol 23(1):20
Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Reiisi S, Pourreza MR et al (2018) GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. Int J Pediatr Otorhinolaryngol 107:121–126
Song MH, Lee HK, Choi JY, Kim S, Bok J, Kim UK (2010) Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPA. Clin Genet 78(6):524–532
Article CAS PubMed Google Scholar
Riazuddin S, Nazli S, Ahmed ZM, Yang Y, Zulfiqar F, Shaikh RS et al (2008) Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. Hum Mutat 29(4):502–511
Article CAS PubMed Google Scholar
Alasti F, Sanati MH, Behrouzifard AH, Sadeghi A, De Brouwer AP, Kremer H et al (2008) A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families. Int J Pediatr Otorhinolaryngol 72(2):249–255
Sugiyama K, Moteki H, Kitajiri S-I, Kitano T, Nishio S-Y, Yamaguchi T et al (2019) Mid-frequency hearing loss is characteristic clinical feature of OTOA-associated hearing loss. Genes 10(9):715
Article CAS PubMed PubMed Central Google Scholar
Mujtaba G, Bukhari I, Fatima A, Naz SA (2012) C343S missense mutation in PJVK causes progressive hearing loss. Gene 504(1):98–101
Article CAS PubMed PubMed Central Google Scholar
Sarmadi A, Nasrniya S, Farsani MS, Narrei S, Nouri Z, Sepehrnejad M et al (2020) A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. BMC Med Genet 21(1):1–9
Alagramam KN, Goodyear RJ, Geng R, Furness DN, Van Aken AF, Marcotti W et al (2011) Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells. PLoS ONE 6(4):e19183
Article CAS PubMed PubMed Central Google Scholar
Usami S-I, Isaka Y, Miyagawa M, Nishio S-Y (2022) Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss. Human Genet 141(3):903–914
Lin J, Zangi M, Kumar TVNH, Shakar Reddy M, Reddy LVR, Sadhukhan SK et al (2021) Synthetic derivatives of ciclopirox are effective inhibitors of cryptococcus neoformans. ACS Omega 6(12):8477–8487
Article CAS PubMed PubMed Central Google Scholar
Gu X, Sun S, Guo L, Lu X, Mei H, Lai C et al (2015) Novel biallelic OTOGL mutations in a Chinese family with moderate non-syndromic sensorineural hearing loss. Int J Pediatr Otorhinolaryngol 79(6):817–820
Pavlenkova Z, Varga L, Borecka S, Karhanek M, Huckova M, Skopkova M et al (2021) Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss. Sci Rep 11(1):22488
Article CAS PubMed PubMed Central Google Scholar
Yariz KO, Duman D, Seco CZ, Dallman J, Huang M, Peters TA et al (2012) Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss. Am J Human Genet 91(5):872–882
Yu S, Choi HJ, Lee JS, Lee HJ, Rim JH, Choi JY et al (2019) A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction. Eur J Med Genet 62(1):81–84
Zangi M, Donald KA, Casals AG, Franson AD, Alice JY, Marker EM et al (2022) Synthetic derivatives of the antifungal drug ciclopirox are active against herpes simplex virus 2. Eur J Med Chem 238:114443
Article CAS PubMed PubMed Central Google Scholar
Safari H, Zeinali M, Alizadeh P, Mahmoudi D (2024) Topical dexamethason effectiveness combined with surgical intervention in patients suffering from chronic subdural hematoma. Interdiscip Neurosurg 37:101984
Avan P, Le Gal S, Michel V, Dupont T, Hardelin J-P, Petit C et al (2019) Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane. Proc Natl Acad Sci 116(51):25948–25957
Article CAS PubMed PubMed Central Google Scholar
Iossifov I, O’roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D et al (2014) The contribution of de novo coding mutations to autism spectrum disorder. Nature 515(7526):216–221
Article CAS PubMed PubMed Central Google Scholar
Asgharzade S, Tabatabaiefar MA, Mohammadi-Asl J, Chaleshtori MH (2018) A nove
留言 (0)