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1.
J Laryngol Otol ; 138(S2): S3-S7, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38247298

RESUMO

BACKGROUND: There is a high prevalence of dizziness, vertigo and balance symptoms in the general population. Symptoms can be generated by many inner-ear vestibular disorders and there are several diagnostic tests available that can help identify the site of the vestibular lesion. There is little consensus on what diagnostic tests are appropriate, with diagnostics either not completed or minimally performed, leading to missed diagnosis, unsatisfactory results for patients and costs to healthcare systems. METHODS: This study explored the literature for different neuro-vestibular diagnostic tests not currently considered in the traditional standard vestibular test battery, and examined how they fit effectively into a patient care pathway to help quickly and succinctly identify vestibular function. RESULTS: A vestibular patient care pathway is presented for acute and subacute presentation of vestibular disorders. CONCLUSION: An accurate diagnosis following a rigorous anamnesis and vestibular testing is paramount for successful management and favourable outcomes.


Assuntos
Tontura , Vertigem , Doenças Vestibulares , Testes de Função Vestibular , Humanos , Doenças Vestibulares/diagnóstico , Testes de Função Vestibular/métodos , Tontura/diagnóstico , Tontura/etiologia , Vertigem/diagnóstico , Equilíbrio Postural/fisiologia , Vestíbulo do Labirinto/fisiopatologia
2.
Audiol Res ; 13(4): 600-614, 2023 Aug 04.
Artigo em Inglês | MEDLINE | ID: mdl-37622928

RESUMO

Conductive hearing losses are typically present in disorders of the external/middle ear. However, there is a rare group of inner ear conditions called third windows that can also generate a conductive hearing loss. This is due to an abnormal connection between the middle and the inner ear or between the inner ear and the cranial cavity. X-linked gusher disorder is an extremely rare congenital inner ear dysplastic syndrome with an abnormal connection due to a characteristic incomplete cochlear partition type III and an incomplete internal auditory meatus fundus. The disorder is inherited in an X-linked fashion due to the mutation of the POU3F4 gene. We present two siblings diagnosed with the condition and their long-term follow-ups. They both presented audiovestibular symptoms and showed progressive mixed losses and bilateral vestibular weakness. They were treated with cochlear implant, digital amplification and with vestibular rehabilitation. Significant others around them were involved in their journey with the medical team, and in both, a very favourable outcome was achieved. This is the first time that we have reported evolving audiovestibular function with vestibular quantification in X-linked gusher disorder and emphasize on the multidisciplinary holistic approach to manage these children effectively.

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