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Newborn genetic screening for hearing impairment: a population-based longitudinal study.
Wu CC, Tsai CH, Hung CC, Lin YH, Lin YH, Huang FL, Tsao PN, Su YN, Lee YL, Hsieh WS, Hsu CJ. Wu CC, et al. Genet Med. 2017 Jan;19(1):6-12. doi: 10.1038/gim.2016.66. Epub 2016 Jun 16. Genet Med. 2017. PMID: 27308839 Free article.
RESULTS: Newborn genetic screening identified 82 (1.6%) babies with conclusive genotypes, comprising 62 (1.2%) with GJB2 p.V37I/p.V37I, 16 (0.3%) with GJB2 p.V37I/c.235delC, and 4 (0.1%) with m.1555A>G. Of these, 46 (56.1%) passed hearing screening at birth. Long-term f …
RESULTS: Newborn genetic screening identified 82 (1.6%) babies with conclusive genotypes, comprising 62 (1.2%) with GJB2 p.V37I/p.V37I, 16 ( …
Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.
Hao Z, Fu D, Ming Y, Yang J, Huang Q, Lin W, Zhang H, Zhang B, Zhou A, Hu X, Yao C, Dong Y, Ring HZ, Ring BZ. Hao Z, et al. PLoS One. 2018 Apr 10;13(4):e0195740. doi: 10.1371/journal.pone.0195740. eCollection 2018. PLoS One. 2018. PMID: 29634755 Free PMC article.
Almost one third of the three million people in China suffering severe deafness are children, and 50% of these cases are believed to have genetic components to their etiology. Newborn hearing genetic screening can complement Universal Neonatal Hearing Screening for …
Almost one third of the three million people in China suffering severe deafness are children, and 50% of these cases are believed to have ge …
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Phenotype-Genotype Study.
Liu XZ, Yan D, Mittal R, Ballard ME, Feng Y. Liu XZ, et al. Laryngoscope. 2020 Jul;130(7):1657-1663. doi: 10.1002/lary.28318. Epub 2019 Oct 8. Laryngoscope. 2020. PMID: 31593348
RESULTS: Progressive hearing impairment was confirmed by history and by audiological follow-up testing in all the patients. ...CONCLUSIONS: Our study and the review of the literature suggest that P2RX2 plays a crucial role in predisposition to noise-induced a …
RESULTS: Progressive hearing impairment was confirmed by history and by audiological follow-up testing in all the patie …
Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center.
Wu CC, Hung CC, Lin SY, Hsieh WS, Tsao PN, Lee CN, Su YN, Hsu CJ. Wu CC, et al. PLoS One. 2011;6(7):e22314. doi: 10.1371/journal.pone.0022314. Epub 2011 Jul 19. PLoS One. 2011. PMID: 21811586 Free PMC article.
Universal newborn hearing screening (UNHS) is of paramount importance for early identification and management of hearing impairment in children. However, infants with slight/mild, progressive, or late-onset hearing impairment might be mis …
Universal newborn hearing screening (UNHS) is of paramount importance for early identification and management of hearing im …
The Conspicuous Link between Ear, Brain and Heart-Could Neurotrophin-Treatment of Age-Related Hearing Loss Help Prevent Alzheimer's Disease and Associated Amyloid Cardiomyopathy?
Shityakov S, Hayashi K, Störk S, Scheper V, Lenarz T, Förster CY. Shityakov S, et al. Biomolecules. 2021 Jun 17;11(6):900. doi: 10.3390/biom11060900. Biomolecules. 2021. PMID: 34204299 Free PMC article. Review.
Of particular interest, it can be demonstrated that Abeta pathology is present in the hearts of patients with AD, while the formation of NFT in the auditory system can be detected much earlier than the onset of symptoms. Progressive hearing impairment may beg …
Of particular interest, it can be demonstrated that Abeta pathology is present in the hearts of patients with AD, while the formation of NFT …
Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China.
Zhang J, Wang P, Han B, Ding Y, Pan L, Zou J, Liu H, Pang X, Liu E, Wang H, Liu H, Zhang X, Cheng X, Feng D, Li Q, Wang D, Zong L, Yi Y, Tian N, Mu F, Tian G, Chen Y, Liu G, Zhang F, Yi X, Yang L, Wang Q. Zhang J, et al. Int J Pediatr Otorhinolaryngol. 2013 Dec;77(12):1929-35. doi: 10.1016/j.ijporl.2013.08.038. Epub 2013 Sep 8. Int J Pediatr Otorhinolaryngol. 2013. PMID: 24100002
However, neonates with late-onset and progressive hearing impairment will be missed by NHS. Genetic factors account for an estimated 60% of congenital profound hearing loss. Our previous cohort studies were carried out in an innovative mode, i.e. he …
However, neonates with late-onset and progressive hearing impairment will be missed by NHS. Genetic factors account for …
Predicting the degree of hearing loss using click auditory brainstem response in babies referred from newborn hearing screening.
Baldwin M, Watkin P. Baldwin M, et al. Ear Hear. 2013 May-Jun;34(3):361-9. doi: 10.1097/AUD.0b013e3182728b88. Ear Hear. 2013. PMID: 23340456
DESIGN: Children with permanent childhood hearing impairment were ascertained from neonatal screening programs that have been subject to longitudinal evaluation. ...RESULTS: Of the 92 children recruited to the study two children had a confirmed auditory neuropathy s …
DESIGN: Children with permanent childhood hearing impairment were ascertained from neonatal screening programs that have been …