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pubmed-article:3755572rdf:typepubmed:Citationlld:pubmed
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pubmed-article:3755572pubmed:issue4lld:pubmed
pubmed-article:3755572pubmed:dateCreated1986-9-17lld:pubmed
pubmed-article:3755572pubmed:abstractTextWe report the case of a profoundly deaf 4-year-old boy with congenital deafness as a result of Mondini's dysplasia. The Mondini inner ear malformation is the result of arrested labyrinthine development during embryogenesis and is characterized by both bony and membranous anomalies of the inner ear. The dysplastic cochlear anatomy does not preclude successful cochlear implantation, and electrical threshold measurements are similar to those recorded in pediatric subjects deafened as a result of other causes.lld:pubmed
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pubmed-article:3755572pubmed:issn0192-9763lld:pubmed
pubmed-article:3755572pubmed:authorpubmed-author:MiyamotoR TRTlld:pubmed
pubmed-article:3755572pubmed:authorpubmed-author:PopeM LMLlld:pubmed
pubmed-article:3755572pubmed:authorpubmed-author:MyresW AWAlld:pubmed
pubmed-article:3755572pubmed:authorpubmed-author:RobbinsA JAJlld:pubmed
pubmed-article:3755572pubmed:issnTypePrintlld:pubmed
pubmed-article:3755572pubmed:volume7lld:pubmed
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pubmed-article:3755572pubmed:pagination258-61lld:pubmed
pubmed-article:3755572pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:3755572pubmed:year1986lld:pubmed
pubmed-article:3755572pubmed:articleTitleCochlear implantation in the Mondini inner ear malformation.lld:pubmed
pubmed-article:3755572pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3755572pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:3755572pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed