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dc.contributor.authorIsmail, Meriam T.-
dc.contributor.authorRahman, Razlina A.-
dc.contributor.authorIdris, Nur S.-
dc.date.accessioned2024-10-31T04:46:43Z-
dc.date.available2024-10-31T04:46:43Z-
dc.date.issued2022-
dc.identifier.issn1658-3612-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/7116-
dc.description.abstractFacial nerve paralysis in children is a rare clinical condition that can lead to serious complications. Due to their rare occurrence, tumours, especially in the cerebellopontine angle, may be overlooked. We report a case of cerebellopontine angle tumour in an 8-year-old boy who presented with a right-sided lower motor neuron type of facial nerve palsy. Further examination showed a mild bilateral nystagmus. However, misled by the initial diagnosis of Bell’s palsy, there was a delay in performing diagnostic magnetic resonance imaging of the brain, which showed a large mass in the cerebellopontine. Subsequently, six weeks after his initial presentation, the boy succumbed to the disease. This case illustrates that careful clinical examination, even in a seemingly simple case, is imperative to avoid diagnostic errors.en_US
dc.language.isoen_USen_US
dc.publisherJournal of Taibah University Medical Sciencesen_US
dc.relation.ispartofseriesCase Report;141-145-
dc.subjectBell’s palsyen_US
dc.subjectCerebellopontine angleen_US
dc.subjectClinical examinationen_US
dc.subjectFacial nerveen_US
dc.subjectNystagmusen_US
dc.titleWhen paediatric facial nerve paralysis is not a Bell’s palsy: A case of cerebellopontine angle tumouren_US
dc.typeArticleen_US
Appears in Collections:Vol 17 No 1 (2022)

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