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Anomalia Congénita Coclear: Tentativa de Relação Embriológica e Anátomo-Funcional

dc.contributor.authorMaurício, JC
dc.contributor.authorBiscoito, L
dc.contributor.authorBranco, G
dc.date.accessioned2014-07-15T22:06:38Z
dc.date.available2014-07-15T22:06:38Z
dc.date.issued1993
dc.description.abstractIn this review of cochlear malformations, 17 cases were studied by CT scan (high resolution-target program) including 10 males and 7 females. The anomaly was bilateral in 12 cases and unilateral in 7 (the latter included 2 Mondini type aplasias and one Michel). The cochlear malformation (whose most frequent expression was the cochlear hypoplasia with 1 or 1 1/2 spires-65% of the cases) was associated to semicircular canals and/or vestibular aqueduct anomaly in 82% of the patients; it was exclusively of the anterior labyrinth in 18% of the cases. A middle ear malformation coexisted in 29%: in 3 cases with malleoincudal dysmorphy only and with tympanic aplasia in 2 others. These cochlear anomalies with CT expression were discussed considering the embryology, in view of a possible gestational dating, moreover relating to the hipocusia type: perceptive or combined.por
dc.identifier.citationActa Med Port. 1993;6(8-9):371-5.por
dc.identifier.urihttp://hdl.handle.net/10400.26/6573
dc.language.isoporpor
dc.peerreviewedyespor
dc.subjectAbnormalities, Multiplepor
dc.subjectCochlea/abnormalitiespor
dc.subjectCóclea/anomalias congénitaspor
dc.subjectAnomalias Congénitas Múltiplaspor
dc.titleAnomalia Congénita Coclear: Tentativa de Relação Embriológica e Anátomo-Funcionalpor
dc.title.alternativeCT study of 17 cases of congenital cochlear abnormality. Embryologic and anatomo-functional relationship]por
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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