Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Newborn hearing screening and genetic testing in 8974 Brazilian neonates
Author: Nivoloni, KDB
da Silva-Costa, SM
Pomilio, MCA
Pereira, T
Lopes, KD
de Moraes, VCS
Alexandrino, F
de Oliveira, CA
Sartorato, EL
Abstract: Objective: An early diagnosis has been a priority in the audiological practice. Identifying hearing loss until 3 months old through Universal Newborn Hearing Screening and intervention before 6 months old, minimize the impact of auditory loss in the health and communication development of these children. However, in the clinical practice, despite the help of the risk indicators in the audiological and etiological diagnosis, the integrated services have come up against the challenge of determining the causes of auditory loss, bearing in mind that approximately 50% of the subjects who have congenital loss do not show risk factors in their clinical history. The current research aims introduce together etiologic and audiological diagnosis of newborns. Methods: We eluted dried blood spots from paper and performed genetic testing for 35delG mutation in 8974 newborns that were also screened for transient otoacoustic emissions (TOAE). In addition, the A1555G and A827G mutations in the MTRNR1 mitochondrial gene were screened in all newborns. Results: We have found 17 individuals who failed in TOAE. Among them, we detected 4 homozygous newborns for 35delG mutation and 3 individuals with A827G mutation in the MTRNR1 mitochondrial gene. The frequency of 35delG carriers was 0.94% [84/8974]. In all 17 individuals who failed in OAE no other mutation besides those mentioned above was found. Conclusions: The results greatly contribute to the public health area indicating the etiologic diagnosis, allowing family counseling as well as the early rehabilitation treatment or surgical intervention. Over time that will help to reduce the costs of rehabilitation considerably. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
Subject: Newborns
Hearing loss
35delG mutation
Mitochondrial mutation
Country: Irlanda
Editor: Elsevier Ireland Ltd
Citation: International Journal Of Pediatric Otorhinolaryngology. Elsevier Ireland Ltd, v. 74, n. 8, n. 926, n. 929, 2010.
Rights: fechado
Identifier DOI: 10.1016/j.ijporl.2010.05.015
Date Issue: 2010
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000279832700016.pdf107.19 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.