Cited 19 times in

Limitations of hearing screening in newborns with PDS mutations

DC Field Value Language
dc.contributor.author최재영-
dc.contributor.author김보경-
dc.contributor.author신중욱-
dc.date.accessioned2014-12-18T08:53:49Z-
dc.date.available2014-12-18T08:53:49Z-
dc.date.issued2013-
dc.identifier.issn0165-5876-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/87151-
dc.description.abstractOBJECTIVES: SLC26A4 (PDS) mutations are common cause of congenital hearing loss in East Asia. Hearing loss caused by PDS mutations tends to have delayed presentation; thus universal newborn hearing screening (UNHS) can be less effective in these patients. We examined the efficiency of newborn hearing screening test in patients with bi-allelic PDS mutations. METHODS: Forty-three patients with sensorineural hearing loss were recruited. Patients had an enlarged vestibular aqueduct and biallelic PDS mutations. Among them, newborn hearing screening test had been performed on 14. The remaining 29 patients did not undergo newborn hearing screening test. Another 15 patients without a PDS mutation but who had sensorineural hearing loss were also recruited as a comparison group. We reviewed the hearing loss history of the children using medical records and parent interviews. RESULTS: Among 14 patients with PDS mutation, four (28.6%) passed newborn hearing screening test in both ears and six (42.9%) passed in one ear. In contrast, only 2 of 15 (13.3%) children without a PDS mutation passed newborn hearing screening test bilaterally. The age at confirmation of bilateral hearing loss in bilateral "pass" patients with PDS mutation was 31.5 ± 17.9 months, which was significantly delayed compared to the age for bilateral "refer" children (1.75 ± 0.96 months) (p<0.05). CONCLUSION: The UNHS is not an accurate tool for predicting long-term hearing loss in patients with PDS mutations. We recommend that genetic screening be combined with UNHS, particularly in communities with a high prevalence of PDS mutations, to better identify children in need of early habilitation.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHChild-
dc.subject.MESHChild, Preschool-
dc.subject.MESHFemale-
dc.subject.MESHGenetic Testing/methods*-
dc.subject.MESHHearing Loss, Sensorineural/diagnosis*-
dc.subject.MESHHearing Loss, Sensorineural/epidemiology-
dc.subject.MESHHearing Loss, Sensorineural/genetics-
dc.subject.MESHHearing Tests-
dc.subject.MESHHumans-
dc.subject.MESHInfant-
dc.subject.MESHInfant, Newborn-
dc.subject.MESHMale-
dc.subject.MESHMembrane Transport Proteins/genetics*-
dc.subject.MESHMutation-
dc.subject.MESHNeonatal Screening/methods*-
dc.subject.MESHPrevalence-
dc.subject.MESHRetrospective Studies-
dc.titleLimitations of hearing screening in newborns with PDS mutations-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Otorhinolaryngology (이비인후과학)-
dc.contributor.googleauthorBo Gyung Kim-
dc.contributor.googleauthorJoong-Wook Shin-
dc.contributor.googleauthorHong-Joon Park-
dc.contributor.googleauthorJung Min Kim-
dc.contributor.googleauthorUn-Kyung Kim-
dc.contributor.googleauthorJae Young Choi-
dc.identifier.doi10.1016/j.ijporl.2013.02.023-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA04173-
dc.contributor.localIdA00507-
dc.contributor.localIdA02158-
dc.relation.journalcodeJ01148-
dc.identifier.eissn1872-8464-
dc.identifier.pmid23523376-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0165587613000839-
dc.subject.keywordPendrin-
dc.subject.keywordPDS-
dc.subject.keywordUniversal newborn hearing screening-
dc.subject.keywordHabilitation-
dc.contributor.alternativeNameChoi, Jae Young-
dc.contributor.alternativeNameKim, Bo Gyung-
dc.contributor.alternativeNameShin, Joong Wook-
dc.contributor.affiliatedAuthorChoi, Jae Young-
dc.contributor.affiliatedAuthorKim, Bo Gyung-
dc.contributor.affiliatedAuthorShin, Joong Wook-
dc.rights.accessRightsnot free-
dc.citation.volume77-
dc.citation.number5-
dc.citation.startPage833-
dc.citation.endPage837-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, Vol.77(5) : 833-837, 2013-
dc.identifier.rimsid32523-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers

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