International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.
Identifieur interne : 003C91 ( Ncbi/Curation ); précédent : 003C90; suivant : 003C92International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.
Auteurs : Bryan J. Liming [États-Unis] ; John Carter [États-Unis] ; Alan Cheng [Australie] ; Daniel Choo [États-Unis] ; John Curotta [Australie] ; Daniela Carvalho [États-Unis] ; John A. Germiller [États-Unis] ; Stephen Hone [Irlande (pays)] ; Margaret A. Kenna [États-Unis] ; Natalie Loundon [France] ; Diego Preciado [États-Unis] ; Anne Schilder ; Brian J. Reilly [États-Unis] ; Stephane Roman [France] ; Julie Strychowsky [Canada] ; Jean-Michel Triglia [France] ; Nancy Young [États-Unis] ; Richard J H. Smith [États-Unis]Source :
- International journal of pediatric otorhinolaryngology [ 1872-8464 ] ; 2016.
Descripteurs français
- KwdFr :
- Dépistage génétique, Dépistage néonatal, Dépistage systématique, Enfant, Enfant d'âge préscolaire, Humains, Mâle, Nourrisson, Nouveau-né, Oto-rhino-laryngologie (normes), Perte d'audition (diagnostic), Perte d'audition (génétique), Pédiatrie (normes), Surdité (diagnostic), Surdité (génétique), Surdité centrale (diagnostic), Surdité centrale (génétique), Surdité de transmission (diagnostic), Surdité de transmission (génétique), Surdité mixte de transmission et neurosensorielle (diagnostic), Surdité mixte de transmission et neurosensorielle (génétique), Surdité neurosensorielle (diagnostic), Surdité neurosensorielle (génétique), Émissions otoacoustiques spontanées.
- MESH :
- diagnostic : Perte d'audition, Surdité, Surdité centrale, Surdité de transmission, Surdité mixte de transmission et neurosensorielle, Surdité neurosensorielle.
- génétique : Perte d'audition, Surdité, Surdité centrale, Surdité de transmission, Surdité mixte de transmission et neurosensorielle, Surdité neurosensorielle.
- normes : Oto-rhino-laryngologie, Pédiatrie.
- Dépistage génétique, Dépistage néonatal, Dépistage systématique, Enfant, Enfant d'âge préscolaire, Humains, Mâle, Nourrisson, Nouveau-né, Émissions otoacoustiques spontanées.
English descriptors
- KwdEn :
- Child, Child, Preschool, Deafness (diagnosis), Deafness (genetics), Genetic Testing, Hearing Loss (diagnosis), Hearing Loss (genetics), Hearing Loss, Central (diagnosis), Hearing Loss, Central (genetics), Hearing Loss, Conductive (diagnosis), Hearing Loss, Conductive (genetics), Hearing Loss, Mixed Conductive-Sensorineural (diagnosis), Hearing Loss, Mixed Conductive-Sensorineural (genetics), Hearing Loss, Sensorineural (diagnosis), Hearing Loss, Sensorineural (genetics), Humans, Infant, Infant, Newborn, Male, Mass Screening, Neonatal Screening, Otoacoustic Emissions, Spontaneous, Otolaryngology (standards), Pediatrics (standards).
- MESH :
- diagnosis : Deafness, Hearing Loss, Hearing Loss, Central, Hearing Loss, Conductive, Hearing Loss, Mixed Conductive-Sensorineural, Hearing Loss, Sensorineural.
- genetics : Deafness, Hearing Loss, Hearing Loss, Central, Hearing Loss, Conductive, Hearing Loss, Mixed Conductive-Sensorineural, Hearing Loss, Sensorineural.
- standards : Otolaryngology, Pediatrics.
- Child, Child, Preschool, Genetic Testing, Humans, Infant, Infant, Newborn, Male, Mass Screening, Neonatal Screening, Otoacoustic Emissions, Spontaneous.
Abstract
To provide recommendations for the workup of hearing loss in the pediatric patient.
DOI: 10.1016/j.ijporl.2016.09.016
PubMed: 27729144
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Anne Schilder<affiliation><nlm:affiliation>Evident, UCL Ear Institute, Royal National Throat, Nose and Ear Hospital, London UK.</nlm:affiliation>
<wicri:noCountry code="subField">London UK</wicri:noCountry>
</affiliation>
Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en">International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.</title>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Pediatric Otolaryngology, La Timone Children's Hospital, Aix-Marseille Universite', Marseille</wicri:regionArea>
<placeName><region type="region">Provence-Alpes-Côte d'Azur</region>
<region type="old region">Provence-Alpes-Côte d'Azur</region>
<settlement type="city">Marseille</settlement>
<settlement type="city">Marseille</settlement>
</placeName>
<orgName type="university">Université d'Aix-Marseille</orgName>
</affiliation>
</author>
<author><name sortKey="Young, Nancy" sort="Young, Nancy" uniqKey="Young N" first="Nancy" last="Young">Nancy Young</name>
<affiliation wicri:level="1"><nlm:affiliation>Division of Otolaryngology-Head and Neck Surgery, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago IL, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Division of Otolaryngology-Head and Neck Surgery, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago IL</wicri:regionArea>
<wicri:noRegion>Chicago IL</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Smith, Richard J H" sort="Smith, Richard J H" uniqKey="Smith R" first="Richard J H" last="Smith">Richard J H. Smith</name>
<affiliation wicri:level="2"><nlm:affiliation>Department of Otolaryngology -Head and Neck Surgery, University of Iowa Health Care, Iowa City, IA, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Otolaryngology -Head and Neck Surgery, University of Iowa Health Care, Iowa City, IA</wicri:regionArea>
<placeName><region type="state">Iowa</region>
</placeName>
</affiliation>
</author>
</analytic>
<series><title level="j">International journal of pediatric otorhinolaryngology</title>
<idno type="eISSN">1872-8464</idno>
<imprint><date when="2016" type="published">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Child</term>
<term>Child, Preschool</term>
<term>Deafness (diagnosis)</term>
<term>Deafness (genetics)</term>
<term>Genetic Testing</term>
<term>Hearing Loss (diagnosis)</term>
<term>Hearing Loss (genetics)</term>
<term>Hearing Loss, Central (diagnosis)</term>
<term>Hearing Loss, Central (genetics)</term>
<term>Hearing Loss, Conductive (diagnosis)</term>
<term>Hearing Loss, Conductive (genetics)</term>
<term>Hearing Loss, Mixed Conductive-Sensorineural (diagnosis)</term>
<term>Hearing Loss, Mixed Conductive-Sensorineural (genetics)</term>
<term>Hearing Loss, Sensorineural (diagnosis)</term>
<term>Hearing Loss, Sensorineural (genetics)</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Male</term>
<term>Mass Screening</term>
<term>Neonatal Screening</term>
<term>Otoacoustic Emissions, Spontaneous</term>
<term>Otolaryngology (standards)</term>
<term>Pediatrics (standards)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Dépistage génétique</term>
<term>Dépistage néonatal</term>
<term>Dépistage systématique</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Humains</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Oto-rhino-laryngologie (normes)</term>
<term>Perte d'audition (diagnostic)</term>
<term>Perte d'audition (génétique)</term>
<term>Pédiatrie (normes)</term>
<term>Surdité (diagnostic)</term>
<term>Surdité (génétique)</term>
<term>Surdité centrale (diagnostic)</term>
<term>Surdité centrale (génétique)</term>
<term>Surdité de transmission (diagnostic)</term>
<term>Surdité de transmission (génétique)</term>
<term>Surdité mixte de transmission et neurosensorielle (diagnostic)</term>
<term>Surdité mixte de transmission et neurosensorielle (génétique)</term>
<term>Surdité neurosensorielle (diagnostic)</term>
<term>Surdité neurosensorielle (génétique)</term>
<term>Émissions otoacoustiques spontanées</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Deafness</term>
<term>Hearing Loss</term>
<term>Hearing Loss, Central</term>
<term>Hearing Loss, Conductive</term>
<term>Hearing Loss, Mixed Conductive-Sensorineural</term>
<term>Hearing Loss, Sensorineural</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Perte d'audition</term>
<term>Surdité</term>
<term>Surdité centrale</term>
<term>Surdité de transmission</term>
<term>Surdité mixte de transmission et neurosensorielle</term>
<term>Surdité neurosensorielle</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Deafness</term>
<term>Hearing Loss</term>
<term>Hearing Loss, Central</term>
<term>Hearing Loss, Conductive</term>
<term>Hearing Loss, Mixed Conductive-Sensorineural</term>
<term>Hearing Loss, Sensorineural</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Perte d'audition</term>
<term>Surdité</term>
<term>Surdité centrale</term>
<term>Surdité de transmission</term>
<term>Surdité mixte de transmission et neurosensorielle</term>
<term>Surdité neurosensorielle</term>
</keywords>
<keywords scheme="MESH" qualifier="normes" xml:lang="fr"><term>Oto-rhino-laryngologie</term>
<term>Pédiatrie</term>
</keywords>
<keywords scheme="MESH" qualifier="standards" xml:lang="en"><term>Otolaryngology</term>
<term>Pediatrics</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child</term>
<term>Child, Preschool</term>
<term>Genetic Testing</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Male</term>
<term>Mass Screening</term>
<term>Neonatal Screening</term>
<term>Otoacoustic Emissions, Spontaneous</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Dépistage génétique</term>
<term>Dépistage néonatal</term>
<term>Dépistage systématique</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Humains</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Émissions otoacoustiques spontanées</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">To provide recommendations for the workup of hearing loss in the pediatric patient.</div>
</front>
</TEI>
</record>
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