Audiologic and radiologic findings in cochlear hypoplasia

Abstract Objective The aim of the current study is to evaluate audiologic and radiologic findings of cochlear hypoplasia which is a subgroup of inner ear malformations. Methods This study was a prospective clinical study and based on voluntary participation from cases with cochlear hypoplasia diagno...

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Veröffentlicht in:Auris, nasus, larynx nasus, larynx, 2017-12, Vol.44 (6), p.655-663
Hauptverfasser: Cinar, Betul Cicek, Batuk, Merve Ozbal, Tahir, Emel, Sennaroglu, Gonca, Sennaroglu, Levent
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container_issue 6
container_start_page 655
container_title Auris, nasus, larynx
container_volume 44
creator Cinar, Betul Cicek
Batuk, Merve Ozbal
Tahir, Emel
Sennaroglu, Gonca
Sennaroglu, Levent
description Abstract Objective The aim of the current study is to evaluate audiologic and radiologic findings of cochlear hypoplasia which is a subgroup of inner ear malformations. Methods This study was a prospective clinical study and based on voluntary participation from cases with cochlear hypoplasia diagnosis. The study was conducted at Hacettepe University, Department of Otolaryngology, Head and Neck Surgery and Department of Audiology. Subjects were selected from an inner ear malformations database. Inclusion criteria were having cochlear hypoplasia for at least one ear. There were 66 subjects with an age range of 12 months and 60 years 5 months. For each subject, pure tone audiometry and tympanometry were applied according to chronological and cognitive age. And also, auditory brainstem response test was applied to when it is need. Subjects’ radiologic results were reevaluated to confirm cochlear hypoplasia, cochlear nerve and cochlear aperture. Results Cochlear hypoplasia types were statistically significantly different in terms of HL degree. This difference was caused by cochlear hypoplasia type IV group being was statistically different from the other three groups. Like with degree of HL, cochlear hypoplasia groups were statistically different from other three groups in terms of type of hearing loss. Cochlear aperture and cochlear nerve status showed variation according to cochlear hypoplasia type but these differences were not statistically approved. Conclusions In the current study, incidence of cochlear hypoplasia was 23.5% in all inner ear malformation. With this study, it was seen that subtypes of cochlear hypoplasia showed variability in terms of degree and type of hearing loss and also cochlear aperture and cochlear nerve status. Especially cochlear hypoplasia type IV differs from other three cochlear hypoplasia types.
doi_str_mv 10.1016/j.anl.2016.12.002
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Methods This study was a prospective clinical study and based on voluntary participation from cases with cochlear hypoplasia diagnosis. The study was conducted at Hacettepe University, Department of Otolaryngology, Head and Neck Surgery and Department of Audiology. Subjects were selected from an inner ear malformations database. Inclusion criteria were having cochlear hypoplasia for at least one ear. There were 66 subjects with an age range of 12 months and 60 years 5 months. For each subject, pure tone audiometry and tympanometry were applied according to chronological and cognitive age. And also, auditory brainstem response test was applied to when it is need. Subjects’ radiologic results were reevaluated to confirm cochlear hypoplasia, cochlear nerve and cochlear aperture. Results Cochlear hypoplasia types were statistically significantly different in terms of HL degree. This difference was caused by cochlear hypoplasia type IV group being was statistically different from the other three groups. Like with degree of HL, cochlear hypoplasia groups were statistically different from other three groups in terms of type of hearing loss. Cochlear aperture and cochlear nerve status showed variation according to cochlear hypoplasia type but these differences were not statistically approved. Conclusions In the current study, incidence of cochlear hypoplasia was 23.5% in all inner ear malformation. With this study, it was seen that subtypes of cochlear hypoplasia showed variability in terms of degree and type of hearing loss and also cochlear aperture and cochlear nerve status. Especially cochlear hypoplasia type IV differs from other three cochlear hypoplasia types.</description><identifier>ISSN: 0385-8146</identifier><identifier>EISSN: 1879-1476</identifier><identifier>DOI: 10.1016/j.anl.2016.12.002</identifier><identifier>PMID: 28087093</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acoustic Impedance Tests ; Adolescent ; Adult ; Audiological evaluation ; Audiometry, Pure-Tone ; Child ; Child, Preschool ; Cochlea - abnormalities ; Cochlea - diagnostic imaging ; Cochlea - physiopathology ; Cochlear aperture ; Cochlear Diseases - congenital ; Cochlear Diseases - diagnostic imaging ; Cochlear Diseases - physiopathology ; Cochlear hypoplasia ; Cochlear implantation ; Cochlear nerve ; Congenital Abnormalities - diagnostic imaging ; Congenital Abnormalities - physiopathology ; Evoked Potentials, Auditory, Brain Stem ; Female ; Hearing Loss, Sensorineural - congenital ; Hearing Loss, Sensorineural - diagnostic imaging ; Hearing Loss, Sensorineural - physiopathology ; Humans ; Infant ; Inner ear malformation ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Otolaryngology ; Prospective Studies ; Severity of Illness Index ; Tomography, X-Ray Computed ; Young Adult</subject><ispartof>Auris, nasus, larynx, 2017-12, Vol.44 (6), p.655-663</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. 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Methods This study was a prospective clinical study and based on voluntary participation from cases with cochlear hypoplasia diagnosis. The study was conducted at Hacettepe University, Department of Otolaryngology, Head and Neck Surgery and Department of Audiology. Subjects were selected from an inner ear malformations database. Inclusion criteria were having cochlear hypoplasia for at least one ear. There were 66 subjects with an age range of 12 months and 60 years 5 months. For each subject, pure tone audiometry and tympanometry were applied according to chronological and cognitive age. And also, auditory brainstem response test was applied to when it is need. Subjects’ radiologic results were reevaluated to confirm cochlear hypoplasia, cochlear nerve and cochlear aperture. Results Cochlear hypoplasia types were statistically significantly different in terms of HL degree. This difference was caused by cochlear hypoplasia type IV group being was statistically different from the other three groups. Like with degree of HL, cochlear hypoplasia groups were statistically different from other three groups in terms of type of hearing loss. Cochlear aperture and cochlear nerve status showed variation according to cochlear hypoplasia type but these differences were not statistically approved. Conclusions In the current study, incidence of cochlear hypoplasia was 23.5% in all inner ear malformation. With this study, it was seen that subtypes of cochlear hypoplasia showed variability in terms of degree and type of hearing loss and also cochlear aperture and cochlear nerve status. Especially cochlear hypoplasia type IV differs from other three cochlear hypoplasia types.</description><subject>Acoustic Impedance Tests</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Audiological evaluation</subject><subject>Audiometry, Pure-Tone</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cochlea - abnormalities</subject><subject>Cochlea - diagnostic imaging</subject><subject>Cochlea - physiopathology</subject><subject>Cochlear aperture</subject><subject>Cochlear Diseases - congenital</subject><subject>Cochlear Diseases - diagnostic imaging</subject><subject>Cochlear Diseases - physiopathology</subject><subject>Cochlear hypoplasia</subject><subject>Cochlear implantation</subject><subject>Cochlear nerve</subject><subject>Congenital Abnormalities - diagnostic imaging</subject><subject>Congenital Abnormalities - physiopathology</subject><subject>Evoked Potentials, Auditory, Brain Stem</subject><subject>Female</subject><subject>Hearing Loss, Sensorineural - congenital</subject><subject>Hearing Loss, Sensorineural - diagnostic imaging</subject><subject>Hearing Loss, Sensorineural - physiopathology</subject><subject>Humans</subject><subject>Infant</subject><subject>Inner ear malformation</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Otolaryngology</subject><subject>Prospective Studies</subject><subject>Severity of Illness Index</subject><subject>Tomography, X-Ray Computed</subject><subject>Young Adult</subject><issn>0385-8146</issn><issn>1879-1476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9rHDEMxU1paLZpP0AvZY69zFSyPTMeCoUQ0j8QyKHt2XhtTeKt197aO4H99vGyaQ499CQJ3ntIPzH2DqFDwOHjpjMxdLy2HfIOgL9gK1Tj1KIch5dsBUL1rUI5nLPXpWwAQIxiesXOuQI1wiRWbLpcnE8h3XnbmOiabJ7H2Ufn411pfGxssveBTG7uD7u0C6Z484adzSYUevtUL9ivL9c_r761N7dfv19d3rRWCr5v5SxkDzD1Vtg1KmeMnNDwuixZcHaWg3FCAjfQg6LeSJiVcSRhPZPAGcUF-3DK3eX0Z6Gy11tfLIVgIqWlaFQDymkc1FileJLanErJNOtd9luTDxpBH4npja7E9JGYRq7rEtXz_il-WW_JPTv-IqqCTycB1SMfPGVdrKdoyflMdq9d8v-N__yP2wYfvTXhNx2obNKSY6WnUZdq0D-OLzt-DAcBgxBcPALH2I_t</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Cinar, Betul Cicek</creator><creator>Batuk, Merve Ozbal</creator><creator>Tahir, Emel</creator><creator>Sennaroglu, Gonca</creator><creator>Sennaroglu, Levent</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20171201</creationdate><title>Audiologic and radiologic findings in cochlear hypoplasia</title><author>Cinar, Betul Cicek ; Batuk, Merve Ozbal ; Tahir, Emel ; Sennaroglu, Gonca ; Sennaroglu, Levent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-4f3450095c3cb18daa491a2002ec0dcf46ad3402a0508e5a40f8ade40bfe31f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acoustic Impedance Tests</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Audiological evaluation</topic><topic>Audiometry, Pure-Tone</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cochlea - abnormalities</topic><topic>Cochlea - diagnostic imaging</topic><topic>Cochlea - physiopathology</topic><topic>Cochlear aperture</topic><topic>Cochlear Diseases - congenital</topic><topic>Cochlear Diseases - diagnostic imaging</topic><topic>Cochlear Diseases - physiopathology</topic><topic>Cochlear hypoplasia</topic><topic>Cochlear implantation</topic><topic>Cochlear nerve</topic><topic>Congenital Abnormalities - diagnostic imaging</topic><topic>Congenital Abnormalities - physiopathology</topic><topic>Evoked Potentials, Auditory, Brain Stem</topic><topic>Female</topic><topic>Hearing Loss, Sensorineural - congenital</topic><topic>Hearing Loss, Sensorineural - diagnostic imaging</topic><topic>Hearing Loss, Sensorineural - physiopathology</topic><topic>Humans</topic><topic>Infant</topic><topic>Inner ear malformation</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Otolaryngology</topic><topic>Prospective Studies</topic><topic>Severity of Illness Index</topic><topic>Tomography, X-Ray Computed</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cinar, Betul Cicek</creatorcontrib><creatorcontrib>Batuk, Merve Ozbal</creatorcontrib><creatorcontrib>Tahir, Emel</creatorcontrib><creatorcontrib>Sennaroglu, Gonca</creatorcontrib><creatorcontrib>Sennaroglu, Levent</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Auris, nasus, larynx</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cinar, Betul Cicek</au><au>Batuk, Merve Ozbal</au><au>Tahir, Emel</au><au>Sennaroglu, Gonca</au><au>Sennaroglu, Levent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Audiologic and radiologic findings in cochlear hypoplasia</atitle><jtitle>Auris, nasus, larynx</jtitle><addtitle>Auris Nasus Larynx</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>44</volume><issue>6</issue><spage>655</spage><epage>663</epage><pages>655-663</pages><issn>0385-8146</issn><eissn>1879-1476</eissn><abstract>Abstract Objective The aim of the current study is to evaluate audiologic and radiologic findings of cochlear hypoplasia which is a subgroup of inner ear malformations. Methods This study was a prospective clinical study and based on voluntary participation from cases with cochlear hypoplasia diagnosis. The study was conducted at Hacettepe University, Department of Otolaryngology, Head and Neck Surgery and Department of Audiology. Subjects were selected from an inner ear malformations database. Inclusion criteria were having cochlear hypoplasia for at least one ear. There were 66 subjects with an age range of 12 months and 60 years 5 months. For each subject, pure tone audiometry and tympanometry were applied according to chronological and cognitive age. And also, auditory brainstem response test was applied to when it is need. Subjects’ radiologic results were reevaluated to confirm cochlear hypoplasia, cochlear nerve and cochlear aperture. Results Cochlear hypoplasia types were statistically significantly different in terms of HL degree. This difference was caused by cochlear hypoplasia type IV group being was statistically different from the other three groups. Like with degree of HL, cochlear hypoplasia groups were statistically different from other three groups in terms of type of hearing loss. Cochlear aperture and cochlear nerve status showed variation according to cochlear hypoplasia type but these differences were not statistically approved. Conclusions In the current study, incidence of cochlear hypoplasia was 23.5% in all inner ear malformation. With this study, it was seen that subtypes of cochlear hypoplasia showed variability in terms of degree and type of hearing loss and also cochlear aperture and cochlear nerve status. Especially cochlear hypoplasia type IV differs from other three cochlear hypoplasia types.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28087093</pmid><doi>10.1016/j.anl.2016.12.002</doi><tpages>9</tpages></addata></record>
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subjects Acoustic Impedance Tests
Adolescent
Adult
Audiological evaluation
Audiometry, Pure-Tone
Child
Child, Preschool
Cochlea - abnormalities
Cochlea - diagnostic imaging
Cochlea - physiopathology
Cochlear aperture
Cochlear Diseases - congenital
Cochlear Diseases - diagnostic imaging
Cochlear Diseases - physiopathology
Cochlear hypoplasia
Cochlear implantation
Cochlear nerve
Congenital Abnormalities - diagnostic imaging
Congenital Abnormalities - physiopathology
Evoked Potentials, Auditory, Brain Stem
Female
Hearing Loss, Sensorineural - congenital
Hearing Loss, Sensorineural - diagnostic imaging
Hearing Loss, Sensorineural - physiopathology
Humans
Infant
Inner ear malformation
Magnetic Resonance Imaging
Male
Middle Aged
Otolaryngology
Prospective Studies
Severity of Illness Index
Tomography, X-Ray Computed
Young Adult
title Audiologic and radiologic findings in cochlear hypoplasia
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