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[PMID]:28688553
[Au] Autor:Fontenot TE; Giardina CK; Teagle HF; Park LR; Adunka OF; Buchman CA; Brown KD; Fitzpatrick DC
[Ad] Endereço:University of North Carolina at Chapel Hill, Department of Otolaryngology, Chapel Hill, NC, United States. Electronic address: tatyana_fontenot@med.unc.edu.
[Ti] Título:Clinical role of electrocochleography in children with auditory neuropathy spectrum disorder.
[So] Source:Int J Pediatr Otorhinolaryngol;99:120-127, 2017 Aug.
[Is] ISSN:1872-8464
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: To assess electrocochleography (ECochG) to tones as an instrument to account for CI speech perception outcomes in children with auditory neuropathy spectrum disorder (ANSD). MATERIALS & METHODS: Children (<18 years) receiving CIs for ANSD (n = 30) and non-ANSD (n = 74) etiologies of hearing loss were evaluated with ECochG using tone bursts (0.25-4 kHz). The total response (TR) is the sum of spectral peaks of responses across frequencies. The compound action potential (CAP) and the auditory nerve neurophonic (ANN) in ECochG waveforms were used to estimate nerve activity and calculate nerve score. Performance on open-set monosyllabic word tests was the outcome measure. Standard statistical methods were applied. RESULTS: On average, TR was larger in ANSD than in non-ANSD subjects. Most ANSD (73.3%) and non-ANSD (87.8%) subjects achieved open-set speech perception; TR accounted for 33% and 20% of variability in the outcomes, respectively. In the ANSD group, the PTA accounted for 69.3% of the variability, but there was no relationship with outcomes in the non-ANSD group. In both populations, nerve score was sensitive in identifying subjects at risk for not acquiring open-set speech perception, while the CAP and the ANN were more specific. CONCLUSION: In both subject groups, the TRs correlated with outcomes but these measures were notably larger in the ANSD group. There was also strong correlation between PTA and speech perception outcome in ANSD group. In both subject populations, weaker evidence of neural activity was related to failure to achieve open-set speech perception.
[Mh] Termos MeSH primário: Audiometria de Resposta Evocada/métodos
Implante Coclear/métodos
Perda Auditiva Central/fisiopatologia
Percepção da Fala/fisiologia
[Mh] Termos MeSH secundário: Adolescente
Criança
Pré-Escolar
Estudos de Coortes
Surdez/fisiopatologia
Surdez/cirurgia
Feminino
Seres Humanos
Lactente
Masculino
Estudos Prospectivos
Doenças do Nervo Vestibulococlear/cirurgia
[Pt] Tipo de publicação:JOURNAL ARTICLE; OBSERVATIONAL STUDY
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170803
[Lr] Data última revisão:
170803
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170710
[St] Status:MEDLINE


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[PMID]:28687817
[Au] Autor:Lin PH; Hsu CJ; Lin YH; Lin YH; Lee HY; Wu CC; Liu TC
[Ad] Endereço:Department of Otolaryngology, National Taiwan University Hospital Yunlin Branch, Yunlin, Taiwan.
[Ti] Título:Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss.
[So] Source:JAMA Otolaryngol Head Neck Surg;143(9):912-919, 2017 Sep 01.
[Is] ISSN:2168-619X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Importance: Pediatric-onset unilateral and asymmetric sensorineural hearing loss (SNHL) is a common condition, but in most patients, the cause remains unclear; thus, determination of the hearing outlook is difficult. Objective: To analyze the etiologic and audiologic characteristics of pediatric-onset unilateral and asymmetric SNHL. Design, Setting, and Participants: In this retrospective cohort study performed from January 1, 2008, through December 31, 2016, patients at a tertiary referral center who were diagnosed with pediatric-onset unilateral or asymmetric SNHL were divided into 3 groups according to their hearing levels: unilateral hearing loss with scaled-out levels (UHL-SO), unilateral hearing loss with residual hearing (UHL-RH), and asymmetric hearing loss (AHL). Main Outcomes and Measures: Basic demographic data, family and medical histories, audiologic results, imaging findings, and genetic results were ascertained and compared among patients of the 3 groups. Results: A total of 133 patients (mean [SD] age, 9.1 [10.9] years; 63 [47.4%] male and 70 [52.6%] female), including 50 with UHL-SO, 42 with UHL-RH, and 41 with AHL, were enrolled for analyses. Of 50 patients with UHL-SO, 49 (98.0%) had stable hearing levels with time, whereas 10 of 42 patients with UHL-RH (23.8%) and 18 of 41 patients with AHL (43.9%) revealed progressive or fluctuating hearing loss. Inner ear malformations detected with temporal bone high-resolution computed tomography, particularly cochlear aperture stenosis, were detected at higher rates in patients with UHL-SO (9 of 31 [29.0%]) and UHL-RH (6 of 24 [25.0%]) than in those with AHL (1 of 30 [3.3%]). In contrast, screening for mutations in 3 common deafness genes-GJB2, SLC26A4, and MTRNR1-achieved definite diagnosis in a higher percentage of patients with AHL (10 of 37 [27.0%]) than patients with UHL-SO (0 of 33) and UHL-RH (1 of 25 [4.0%]). Conclusions and Relevance: The UHL-SO and UHL-RH conditions share a common or similar etiopathogenesis different from that of AHL. Imaging studies and genetic testing might be prioritized during the respective general etiologic workups for patients with UHL and AHL. Regular hearing checkups are warranted for patients with UHL and AHL because a certain proportion of patients might sustain progression in SNHL.
[Mh] Termos MeSH primário: Perda Auditiva Neurossensorial/etiologia
Perda Auditiva Unilateral/etiologia
[Mh] Termos MeSH secundário: Criança
Doenças Cocleares/diagnóstico por imagem
Estudos de Coortes
Conexinas/genética
Constrição Patológica/diagnóstico por imagem
Orelha Interna/anormalidades
Orelha Interna/diagnóstico por imagem
Feminino
Testes Genéticos
Seres Humanos
Masculino
Proteínas de Membrana Transportadoras/genética
Mutação
Estudos Retrospectivos
Osso Temporal/diagnóstico por imagem
Doenças do Nervo Vestibulococlear/diagnóstico por imagem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Connexins); 0 (DFNA3 protein, human); 0 (Membrane Transport Proteins); 0 (SLC26A4 protein, human)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171002
[Lr] Data última revisão:
171002
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170709
[St] Status:MEDLINE
[do] DOI:10.1001/jamaoto.2017.0945


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[PMID]:27746081
[Au] Autor:Willms JF; Baltsavias G; Burkhardt JK; Ernst S; Tarnutzer AA
[Ad] Endereço:Department of Neurosurgery, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
[Ti] Título:Missed Anterior Inferior Cerebellar Artery Aneurysm Mimicking Vestibular Neuritis-Clues to Prevent Misdiagnosis.
[So] Source:J Stroke Cerebrovasc Dis;25(12):e231-e232, 2016 Dec.
[Is] ISSN:1532-8511
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:We discuss a case with combined vestibulocochlear and facial neuropathy mimicking a less urgent peripheral vestibular pattern of acute vestibular syndrome (AVS). With initial magnetic resonance imaging read as normal, the patient was treated for vestibular neuropathy until headaches worsened and a diagnosis of subarachnoid hemorrhage was made. On conventional angiography, a ruptured distal right-sided aneurysm of the anterior inferior cerebellar artery was diagnosed and coiled. Whereas acute vestibular loss usually points to a benign peripheral cause of AVS, combined neuropathy of the vestibulocochlear and the facial nerve requires immediate neuroimaging focusing on the cerebellopontine angle. Imaging should be assessed jointly by neuroradiologists and the clinicians in charge to take the clinical context into account.
[Mh] Termos MeSH primário: Aneurisma Roto/diagnóstico por imagem
Cerebelo/irrigação sanguínea
Angiografia Cerebral/métodos
Artérias Cerebrais/diagnóstico por imagem
Erros de Diagnóstico
Aneurisma Intracraniano/diagnóstico por imagem
Neuronite Vestibular/diagnóstico por imagem
[Mh] Termos MeSH secundário: Idoso de 80 Anos ou mais
Aneurisma Roto/complicações
Aneurisma Roto/terapia
Angiografia Digital
Embolização Terapêutica/instrumentação
Doenças do Nervo Facial/etiologia
Evolução Fatal
Feminino
Seres Humanos
Aneurisma Intracraniano/complicações
Aneurisma Intracraniano/terapia
Angiografia por Ressonância Magnética
Valor Preditivo dos Testes
Resultado do Tratamento
Doenças do Nervo Vestibulococlear/etiologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170410
[Lr] Data última revisão:
170410
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161018
[St] Status:MEDLINE


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[PMID]:27647022
[Au] Autor:Esposito G; Messina R; Carai A; Colafati GS; Savioli A; Randi F; De Benedictis A; Cossu S; Fontanella MM; Marras CE
[Ad] Endereço:Neurosurgery Unit, Department of Neuroscience and Neurorehabilitation, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
[Ti] Título:Cochleovestibular Nerve Compression Syndrome Caused by Intrameatal Anterior Inferior Cerebellar Artery Loop: Synthesis of Best Evidence for Clinical Decisions.
[So] Source:World Neurosurg;96:556-561, 2016 Dec.
[Is] ISSN:1878-8769
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:INTRODUCTION: Intrameatal cochleovestibular neurovascular conflict is a rare condition with specific clinical and therapeutic implications. Although surgery is commonly indicated in other neurovascular conflicts, for this subset of patients there is little evidence to guide treatment decisions. Moving from a case description, we performed a review of the literature on this topic to systematically present the best available evidence to guide clinical decisions. METHODS: We performed a literature review on reported cases of surgically treated intrameatal anterior inferior cerebellar artery (AICA)-cochleovestibular nerve neurovascular conflict, analyzing preoperative clinical data, surgical techniques, and outcomes. We analyzed the levels of evidence using the King's College guidelines. DISCUSSION: We found 35 studies of neurovascular compression of the cochleovestibular nerve by AICA for 536 patients operated on to resolve their neurovascular conflict. Only 4 of these studies describe intrameatal AICA neurovascular conflicts, for 9 cases, including our own. Tinnitus was the most frequent symptom (9/9), followed by vertigo (2/9). Our case was the only one showing unilateral hearing loss. Surgery consisted of microsurgical mobilization of the AICA loop performed through a retrosigmoid craniotomy. Tinnitus and vertigo resolved after surgery in all cases, whereas hearing loss did not improve after surgery. CONCLUSIONS: Surgical treatment offers the best results for tinnitus and vertigo, but it seems to have no effect on hearing loss, not even at long-term follow-up. Microvascular decompression should be proposed to intrameatal symptomatic patients before the onset of hearing loss.
[Mh] Termos MeSH primário: Cirurgia de Descompressão Microvascular/efeitos adversos
Síndromes de Compressão Nervosa/cirurgia
Doenças do Nervo Vestibulococlear/cirurgia
Nervo Vestibulococlear/cirurgia
[Mh] Termos MeSH secundário: Comissura Anterior do Cerebelo/patologia
Seres Humanos
PubMed/estatística & dados numéricos
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170912
[Lr] Data última revisão:
170912
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160921
[St] Status:MEDLINE


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[PMID]:27600399
[Au] Autor:Lang H; Nishimoto E; Xing Y; Brown LN; Noble KV; Barth JL; LaRue AC; Ando K; Schulte BA
[Ad] Endereço:Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
[Ti] Título:Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss.
[So] Source:Mol Ther;24(11):2000-2011, 2016 Nov.
[Is] ISSN:1525-0024
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The peripheral auditory nerve (AN) carries sound information from sensory hair cells to the brain. The present study investigated the contribution of mouse and human hematopoietic stem cells (HSCs) to cellular diversity in the AN following the destruction of neuron cell bodies, also known as spiral ganglion neurons (SGNs). Exposure of the adult mouse cochlea to ouabain selectively killed type I SGNs and disrupted the blood-labyrinth barrier. This procedure also resulted in the upregulation of genes associated with hematopoietic cell homing and differentiation, and provided an environment conducive to the tissue engraftment of circulating stem/progenitor cells into the AN. Experiments were performed using both a mouse-mouse bone marrow transplantation model and a severely immune-incompetent mouse model transplanted with human CD34 cord blood cells. Quantitative immunohistochemical analysis of recipient mice demonstrated that ouabain injury promoted an increase in the number of both HSC-derived macrophages and HSC-derived nonmacrophages in the AN. Although rare, a few HSC-derived cells in the injured AN exhibited glial-like qualities. These results suggest that human hematopoietic cells participate in remodeling of the AN after neuron cell body loss and that hematopoietic cells can be an important resource for promoting AN repair/regeneration in the adult inner ear.
[Mh] Termos MeSH primário: Nervo Coclear/efeitos dos fármacos
Células-Tronco Hematopoéticas/citologia
Ouabaína/efeitos adversos
Doenças do Nervo Vestibulococlear/terapia
[Mh] Termos MeSH secundário: Animais
Antígenos CD34/metabolismo
Diferenciação Celular
Nervo Coclear/lesões
Transplante de Células-Tronco de Sangue do Cordão Umbilical
Modelos Animais de Doenças
Sangue Fetal/imunologia
Transplante de Células-Tronco Hematopoéticas
Seres Humanos
Camundongos
Doenças do Nervo Vestibulococlear/induzido quimicamente
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antigens, CD34); 5ACL011P69 (Ouabain)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170531
[Lr] Data última revisão:
170531
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160908
[St] Status:MEDLINE
[do] DOI:10.1038/mt.2016.174


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[PMID]:27367356
[Au] Autor:Kryukov AI; Kunel'skaya NL; Garov EV; Mishchenko VV
[Ad] Endereço:L.I. Sverzhevsky Research Clinical Institute of Otorhinolaryngology, Moscow Health Department, Moscow, Russia, 171152.
[Ti] Título:[The clinical manifestation of the neurovascular conflict of the vestibulocochlear nerve].
[So] Source:Vestn Otorinolaringol;81(3):67-68, 2016.
[Is] ISSN:0042-4668
[Cp] País de publicação:Russia (Federation)
[La] Idioma:rus
[Mh] Termos MeSH primário: Artérias/anormalidades
Malformações Vasculares do Sistema Nervoso Central
Cerebelo/irrigação sanguínea
Síndromes de Compressão Nervosa
Doenças do Nervo Vestibulococlear
Nervo Vestibulococlear/patologia
[Mh] Termos MeSH secundário: Malformações Vasculares do Sistema Nervoso Central/complicações
Malformações Vasculares do Sistema Nervoso Central/diagnóstico
Malformações Vasculares do Sistema Nervoso Central/fisiopatologia
Diagnóstico Diferencial
Seres Humanos
Imagem por Ressonância Magnética/métodos
Masculino
Meia-Idade
Síndromes de Compressão Nervosa/diagnóstico
Síndromes de Compressão Nervosa/etiologia
Síndromes de Compressão Nervosa/fisiopatologia
Tomografia Computadorizada por Raios X/métodos
Doenças do Nervo Vestibulococlear/diagnóstico
Doenças do Nervo Vestibulococlear/etiologia
Doenças do Nervo Vestibulococlear/fisiopatologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1609
[Cu] Atualização por classe:170621
[Lr] Data última revisão:
170621
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160702
[St] Status:MEDLINE
[do] DOI:10.17116/otorino201681367-68


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[PMID]:27203843
[Au] Autor:Fang CH; Chung SY; Blake DM; Vazquez A; Li C; Carey JP; Francis HW; Jyung RW
[Ad] Endereço:*Department of Otolaryngology-Head and Neck Surgery, Albert Einstein College of Medicine, Bronx, New York †Department of Otolaryngology-Head and Neck Surgery, Rutgers New Jersey Medical School, Newark, New Jersey ‡Department of Otolaryngology-Head and Neck Surgery, University of Connecticut School of Medicine, Farmington, Connecticut §Department of Statistics and Biostatistics, Rutgers University, Piscataway, New Jersey ||Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
[Ti] Título:Prevalence of Cochlear-Facial Dehiscence in a Study of 1,020 Temporal Bone Specimens.
[So] Source:Otol Neurotol;37(7):967-72, 2016 Aug.
[Is] ISSN:1537-4505
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: To determine the prevalence of cochlear-facial dehiscence (CFD) and to examine the influence of otic capsule area, age, sex, and race on CFD. STUDY DESIGN: Descriptive study of archived temporal bone specimens. MATERIALS AND METHODS: Targeted sections from 1,020 temporal bone specimens were scanned and examined for CFD. Cochlear-facial partition width (CFPW) and otic capsule area (OCA), a marker of bone thickness, were measured using image analysis software. Demographic data were analyzed using multiple linear regression analysis. RESULTS: The mean CFPW was 0.23 mm (range, 0-0.92 mm; SD, 0.15 mm). Six patients were completely dehiscent (0.59%). Fallopian canal width, age, sex, race, and OCA were found to be significant predictors of CFPW. Age was found to be negatively correlated with CFPW (ß = -0.001) (p < 0.005). Thicker CFPW was associated with males (ß = 0.024) and non-Caucasian individuals (ß = 0.031). The mean OCA for dehiscent specimens (mean, 9.48 mm; range, 6.65-11.58 mm; SD 3.21 mm) was significantly smaller than the mean OCA for nondehiscent specimens, (mean, 12.88 mm; range, 6.63-21.92 mm; SD, 2.47 mm) (p < 0.01). CONCLUSION: CFD occurred in nearly 0.6% of specimens in this temporal bone collection. Close to 35% of patients were sufficiently thin (<0.1 mm) to appear dehiscent on computed tomography scanning. Smaller OCA correlated with thinner CFPW, suggesting a developmental factor. Older, female, and Caucasian patients may have a greater risk for CFD and its associated symptoms.
[Mh] Termos MeSH primário: Nervo Coclear/patologia
Doenças do Nervo Facial/epidemiologia
Nervo Facial/patologia
Doenças do Nervo Vestibulococlear/epidemiologia
[Mh] Termos MeSH secundário: Feminino
Seres Humanos
Masculino
Prevalência
Osso Temporal/anatomia & histologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170908
[Lr] Data última revisão:
170908
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160521
[St] Status:MEDLINE
[do] DOI:10.1097/MAO.0000000000001057


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[PMID]:27187111
[Au] Autor:Chao X; Luo J; Fan Z; Shi H; Han Y; Wang R; Song Y; Wang G; Wang H; Xu L
[Ad] Endereço:a Department of Otolaryngology Head and Neck Surgery , Shandong Provincial Hospital Affiliated to Shandong University; Eye & Ear Infirmary of Shandong Provincial Hospital Group , Shandong , PR China ;
[Ti] Título:Usefulness of radiological findings for predicting cochlear implantation outcomes in children with cochlear nerve deficiency: a pilot study.
[So] Source:Acta Otolaryngol;136(10):1051-7, 2016 Oct.
[Is] ISSN:1651-2251
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:CONCLUSION: Children with CND received limited benefits from CIs and their results varied. The size of the vestibulocochlear nerve relative to the facial nerve could potentially be used as a predicator for CI outcomes in children with CND. OBJECTIVE: This study aimed to (1) retrospectively review the outcomes of cochlear implants (CIs) in children with cochlear nerve deficiency (CND) and (2) evaluate the clinical usefulness of radiological findings as predictors for post-implantation outcomes. METHODS: Study participants included 10 children with bilateral CND and profound sensorineural hearing loss. The preoperative magnetic resonance imaging and temporal bone computed tomography scans were evaluated. Auditory processing capability and speech perception performance were measured with Categories of Auditory Performance (CAP) and Speech Intelligibility Rating (SIR) scales. Aided hearing thresholds with CI were measured. The relationships between CI outcomes and the sizes of vestibulocochlear nerve and cochlear nerve canal (CNC) were analysed. RESULTS: Although post-operative CAP scores and hearing thresholds significantly improved in children with CND, their results were worse than those measured in implanted children with normal cochlear nerve. No significant correlation was found between the CI outcomes and the vestibulocochlear nerve diameters or the CNC diameters in children with CND. However, children with larger vestibulocochlear-nerve-to-facial-nerve-ratios got better results.
[Mh] Termos MeSH primário: Implante Coclear
Doenças do Nervo Vestibulococlear/cirurgia
[Mh] Termos MeSH secundário: Criança
Pré-Escolar
Feminino
Seres Humanos
Lactente
Imagem por Ressonância Magnética
Masculino
Estudos Retrospectivos
Tomografia Computadorizada por Raios X
Resultado do Tratamento
Doenças do Nervo Vestibulococlear/diagnóstico por imagem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1702
[Cu] Atualização por classe:170216
[Lr] Data última revisão:
170216
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160518
[St] Status:MEDLINE
[do] DOI:10.1080/00016489.2016.1179788


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[PMID]:26902641
[Au] Autor:Mesquita EC; Rouanet C; Lucas GL; de Lemos Ados S; Lima MA
[Ad] Endereço:Centro de Referência para Imunobiológicos Especiais, Rio de Janeiro, Brazil. Electronic address: emersom.mesquita@ini.fiocruz.br.
[Ti] Título:Acute bilateral vestibulocochlear neuritis following cultured cell vaccine administration for rabies post-exposure prophylaxis.
[So] Source:J Neurol Sci;364:198-9, 2016 May 15.
[Is] ISSN:1878-5883
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Mh] Termos MeSH primário: Profilaxia Pós-Exposição/métodos
Vacinas Antirrábicas/uso terapêutico
Doenças do Nervo Vestibulococlear/imunologia
Doenças do Nervo Vestibulococlear/terapia
[Mh] Termos MeSH secundário: Células Cultivadas
Feminino
Seres Humanos
Meia-Idade
Raiva
[Pt] Tipo de publicação:CASE REPORTS; LETTER
[Nm] Nome de substância:
0 (Rabies Vaccines)
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170110
[Lr] Data última revisão:
170110
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160224
[St] Status:MEDLINE


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[PMID]:26691155
[Au] Autor:Chetcuti K; Kumbla S
[Ad] Endereço:Department of Medical Imaging, The Royal Children's Hospital, Flemington Road, Parkville, VIC, 3052, Australia. karenchetcuti212@yahoo.co.uk.
[Ti] Título:The internal acoustic canal--another review area in paediatric sensorineural hearing loss.
[So] Source:Pediatr Radiol;46(4):562-9, 2016 Apr.
[Is] ISSN:1432-1998
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Morphological abnormalities of the internal acoustic canal (IAC), albeit rare, are sometimes associated with hearing loss in children. We present an illustration of the spectrum of IAC abnormalities together with a brief review of the embryology and anatomy of the IAC and the techniques used when imaging the petrous temporal bone. This review focuses on morphological abnormalities of the IAC together with their clinical implications and impact on clinical management.
[Mh] Termos MeSH primário: Perda Auditiva Neurossensorial/diagnóstico por imagem
Perda Auditiva Neurossensorial/etiologia
Síndromes de Compressão Nervosa/etiologia
Osso Temporal/anormalidades
Osso Temporal/diagnóstico por imagem
Doenças do Nervo Vestibulococlear/etiologia
[Mh] Termos MeSH secundário: Criança
Pré-Escolar
Feminino
Perda Auditiva Neurossensorial/patologia
Seres Humanos
Imagem por Ressonância Magnética/métodos
Masculino
Síndromes de Compressão Nervosa/diagnóstico por imagem
Síndromes de Compressão Nervosa/patologia
Osso Temporal/patologia
Tomografia Computadorizada por Raios X/métodos
Doenças do Nervo Vestibulococlear/diagnóstico por imagem
Doenças do Nervo Vestibulococlear/patologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1612
[Cu] Atualização por classe:170922
[Lr] Data última revisão:
170922
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151223
[St] Status:MEDLINE
[do] DOI:10.1007/s00247-015-3496-4



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