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Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review
Enlarged Vestibular Aqueduct Syndrome is characterized by a widening of the vestibular aqueduct, associated with sensorineural hearing loss, or sometimes with mixed hearing loss, which may be congenital or acquired during childhood. The sensorineural hearing loss may be classified into mild, moderat...
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Published in: | Brazilian journal of otorhinolaryngology 2005-05, Vol.71 (3), p.386-391 |
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container_title | Brazilian journal of otorhinolaryngology |
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creator | Pinto, José A. Mello, Carlos Fernando Marqui, Ana Carla S. Perfeito, Delmer J. Ferreira, Roberto D.P. Silva, Rubens H. |
description | Enlarged Vestibular Aqueduct Syndrome is characterized by a widening of the vestibular aqueduct, associated with sensorineural hearing loss, or sometimes with mixed hearing loss, which may be congenital or acquired during childhood. The sensorineural hearing loss may be classified into mild, moderate and severe, associated with sudden periods of improvement or aggravation. The enlargement of the vestibular aqueduct is the most common inner ear anomaly. This syndrome is admitted as a result of a genetic abnormality of the vestibular aqueduct development, previous to the fifth week of gestation. The incidence of this syndrome ranges from 1% to 1.3%, with the possibility of getting up to 7%, depending on the examined population. The aim of this study was to analyze three cases of LVAS seen at the Otorhinolaryngology and Radiology Department of Sao Camilo Hospital - Sao Paulo. Two of these three cases were of brothers, from the same mother but from different fathers. Two were male and one was female and the ages ranged from 9 to 30 years old. The diagnostic method of election was CT - Computerized Tomography of the temporal bones. The recommended management of the cases was conservative, except for those of cranial trauma, barotrauma and, if necessary, the use of hearing aids. |
doi_str_mv | 10.1016/S1808-8694(15)31342-2 |
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The sensorineural hearing loss may be classified into mild, moderate and severe, associated with sudden periods of improvement or aggravation. The enlargement of the vestibular aqueduct is the most common inner ear anomaly. This syndrome is admitted as a result of a genetic abnormality of the vestibular aqueduct development, previous to the fifth week of gestation. The incidence of this syndrome ranges from 1% to 1.3%, with the possibility of getting up to 7%, depending on the examined population. The aim of this study was to analyze three cases of LVAS seen at the Otorhinolaryngology and Radiology Department of Sao Camilo Hospital - Sao Paulo. Two of these three cases were of brothers, from the same mother but from different fathers. Two were male and one was female and the ages ranged from 9 to 30 years old. The diagnostic method of election was CT - Computerized Tomography of the temporal bones. The recommended management of the cases was conservative, except for those of cranial trauma, barotrauma and, if necessary, the use of hearing aids.</description><identifier>ISSN: 1808-8694</identifier><identifier>EISSN: 1808-8686</identifier><identifier>DOI: 10.1016/S1808-8694(15)31342-2</identifier><identifier>PMID: 16446948</identifier><language>eng</language><publisher>Brazil: Elsevier Editora Ltda</publisher><subject>Adolescent ; Adult ; Age Factors ; Case Report ; Child ; Cochlear Implantation ; Diagnosis, Differential ; enlarged vestibular aqueduct ; Female ; floating sensorineural hearing loss ; Hearing Loss, Sensorineural - diagnosis ; Hearing Loss, Sensorineural - genetics ; Hearing Loss, Sensorineural - therapy ; Humans ; Male ; mixed hearing loss ; Syndrome ; Tomography, X-Ray Computed ; Vestibular Aqueduct - diagnostic imaging ; Vestibular Diseases - diagnosis ; Vestibular Diseases - genetics ; Vestibular Diseases - therapy</subject><ispartof>Brazilian journal of otorhinolaryngology, 2005-05, Vol.71 (3), p.386-391</ispartof><rights>2005 Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2792-4d913a75eb2161bcf31c2bbb1bd56ee0565926edbc30915fd321f1ce6fcab2953</citedby><cites>FETCH-LOGICAL-c2792-4d913a75eb2161bcf31c2bbb1bd56ee0565926edbc30915fd321f1ce6fcab2953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450622/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1808869415313422$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3549,27924,27925,45780,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16446948$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pinto, José A.</creatorcontrib><creatorcontrib>Mello, Carlos Fernando</creatorcontrib><creatorcontrib>Marqui, Ana Carla S.</creatorcontrib><creatorcontrib>Perfeito, Delmer J.</creatorcontrib><creatorcontrib>Ferreira, Roberto D.P.</creatorcontrib><creatorcontrib>Silva, Rubens H.</creatorcontrib><title>Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review</title><title>Brazilian journal of otorhinolaryngology</title><addtitle>Braz J Otorhinolaryngol</addtitle><description>Enlarged Vestibular Aqueduct Syndrome is characterized by a widening of the vestibular aqueduct, associated with sensorineural hearing loss, or sometimes with mixed hearing loss, which may be congenital or acquired during childhood. The sensorineural hearing loss may be classified into mild, moderate and severe, associated with sudden periods of improvement or aggravation. The enlargement of the vestibular aqueduct is the most common inner ear anomaly. This syndrome is admitted as a result of a genetic abnormality of the vestibular aqueduct development, previous to the fifth week of gestation. The incidence of this syndrome ranges from 1% to 1.3%, with the possibility of getting up to 7%, depending on the examined population. The aim of this study was to analyze three cases of LVAS seen at the Otorhinolaryngology and Radiology Department of Sao Camilo Hospital - Sao Paulo. Two of these three cases were of brothers, from the same mother but from different fathers. Two were male and one was female and the ages ranged from 9 to 30 years old. The diagnostic method of election was CT - Computerized Tomography of the temporal bones. The recommended management of the cases was conservative, except for those of cranial trauma, barotrauma and, if necessary, the use of hearing aids.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Case Report</subject><subject>Child</subject><subject>Cochlear Implantation</subject><subject>Diagnosis, Differential</subject><subject>enlarged vestibular aqueduct</subject><subject>Female</subject><subject>floating sensorineural hearing loss</subject><subject>Hearing Loss, Sensorineural - diagnosis</subject><subject>Hearing Loss, Sensorineural - genetics</subject><subject>Hearing Loss, Sensorineural - therapy</subject><subject>Humans</subject><subject>Male</subject><subject>mixed hearing loss</subject><subject>Syndrome</subject><subject>Tomography, X-Ray Computed</subject><subject>Vestibular Aqueduct - diagnostic imaging</subject><subject>Vestibular Diseases - diagnosis</subject><subject>Vestibular Diseases - genetics</subject><subject>Vestibular Diseases - therapy</subject><issn>1808-8694</issn><issn>1808-8686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkElPwzAQhS0EYin8BJCPcAh4nNhNOIBQVRapggNwtrxMilGbFDsp6r8nXcRy4uTxzHtvNB8hx8DOgYG8eIac5Ukui-wUxFkKacYTvkX2N-1cbn_XRbZHDmJ8Z0z2WV_skj2QWda1833yOKwmOozR0TnGxpu2-1H90aJrbUPjonKhnuIlDTirQ0PrkqbU6oiR6srRiW8w6KYN2AnmHj8PyU6pJxGPNm-PvN4OXwb3yejp7mFwM0os7xc8yVwBqe4LNBwkGFumYLkxBowTEpEJKQou0RmbsgJE6VIOJViUpdWGFyLtkat17qw1U3QWqyboiZoFP9VhoWrt1d9J5d_UuJ6rIhNMct4FiHWADXWMActvLzC1BKxWgNWSngKhVoDV0nfye_GPa0O0E1yvBdid3yEJKlqPlUXnA9pGudr_s-IL6SaNcQ</recordid><startdate>200505</startdate><enddate>200505</enddate><creator>Pinto, José A.</creator><creator>Mello, Carlos Fernando</creator><creator>Marqui, Ana Carla S.</creator><creator>Perfeito, Delmer J.</creator><creator>Ferreira, Roberto D.P.</creator><creator>Silva, Rubens H.</creator><general>Elsevier Editora Ltda</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>5PM</scope></search><sort><creationdate>200505</creationdate><title>Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review</title><author>Pinto, José A. ; Mello, Carlos Fernando ; Marqui, Ana Carla S. ; Perfeito, Delmer J. ; Ferreira, Roberto D.P. ; Silva, Rubens H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2792-4d913a75eb2161bcf31c2bbb1bd56ee0565926edbc30915fd321f1ce6fcab2953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Case Report</topic><topic>Child</topic><topic>Cochlear Implantation</topic><topic>Diagnosis, Differential</topic><topic>enlarged vestibular aqueduct</topic><topic>Female</topic><topic>floating sensorineural hearing loss</topic><topic>Hearing Loss, Sensorineural - diagnosis</topic><topic>Hearing Loss, Sensorineural - genetics</topic><topic>Hearing Loss, Sensorineural - therapy</topic><topic>Humans</topic><topic>Male</topic><topic>mixed hearing loss</topic><topic>Syndrome</topic><topic>Tomography, X-Ray Computed</topic><topic>Vestibular Aqueduct - diagnostic imaging</topic><topic>Vestibular Diseases - diagnosis</topic><topic>Vestibular Diseases - genetics</topic><topic>Vestibular Diseases - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pinto, José A.</creatorcontrib><creatorcontrib>Mello, Carlos Fernando</creatorcontrib><creatorcontrib>Marqui, Ana Carla S.</creatorcontrib><creatorcontrib>Perfeito, Delmer J.</creatorcontrib><creatorcontrib>Ferreira, Roberto D.P.</creatorcontrib><creatorcontrib>Silva, Rubens H.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brazilian journal of otorhinolaryngology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pinto, José A.</au><au>Mello, Carlos Fernando</au><au>Marqui, Ana Carla S.</au><au>Perfeito, Delmer J.</au><au>Ferreira, Roberto D.P.</au><au>Silva, Rubens H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review</atitle><jtitle>Brazilian journal of otorhinolaryngology</jtitle><addtitle>Braz J Otorhinolaryngol</addtitle><date>2005-05</date><risdate>2005</risdate><volume>71</volume><issue>3</issue><spage>386</spage><epage>391</epage><pages>386-391</pages><issn>1808-8694</issn><eissn>1808-8686</eissn><abstract>Enlarged Vestibular Aqueduct Syndrome is characterized by a widening of the vestibular aqueduct, associated with sensorineural hearing loss, or sometimes with mixed hearing loss, which may be congenital or acquired during childhood. The sensorineural hearing loss may be classified into mild, moderate and severe, associated with sudden periods of improvement or aggravation. The enlargement of the vestibular aqueduct is the most common inner ear anomaly. This syndrome is admitted as a result of a genetic abnormality of the vestibular aqueduct development, previous to the fifth week of gestation. The incidence of this syndrome ranges from 1% to 1.3%, with the possibility of getting up to 7%, depending on the examined population. The aim of this study was to analyze three cases of LVAS seen at the Otorhinolaryngology and Radiology Department of Sao Camilo Hospital - Sao Paulo. Two of these three cases were of brothers, from the same mother but from different fathers. Two were male and one was female and the ages ranged from 9 to 30 years old. The diagnostic method of election was CT - Computerized Tomography of the temporal bones. 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subjects | Adolescent Adult Age Factors Case Report Child Cochlear Implantation Diagnosis, Differential enlarged vestibular aqueduct Female floating sensorineural hearing loss Hearing Loss, Sensorineural - diagnosis Hearing Loss, Sensorineural - genetics Hearing Loss, Sensorineural - therapy Humans Male mixed hearing loss Syndrome Tomography, X-Ray Computed Vestibular Aqueduct - diagnostic imaging Vestibular Diseases - diagnosis Vestibular Diseases - genetics Vestibular Diseases - therapy |
title | Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review |
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