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488 Possible Causes for Vestibular Dysfunction

  • Vestibular Neuronitis

    Objectives: To assess the effectiveness of corticosteroids in the management of patients with idiopathic acute vestibular dysfunction (vestibular neuritis).[cochrane.org] Abstract The square drawing test (SDT) devised by Sekitani (1975), which is a modification of Fukuda's vertical writing test, was performed to evaluate vestibular dysfunction[ncbi.nlm.nih.gov] dysfunction.[cochrane.org]

  • Autosomal Recessive Deafness 1B

    Pendred syndrome (PS) is the second most common type of autosomal recessive syndromic hearing loss (HL). It is characterised by sensorineural HL and goiter with occasional hypothyroidism. These features are generally accompanied by malformations of the inner ear, as enlarged vestibular aqueduct (EVA). In about[…][ncbi.nlm.nih.gov]

  • Usher Syndrome Type I

    Usher syndrome type I (USH1) is characterised by profound congenital sensorineural hearing loss, vestibular dysfunction, and prepubertal onset of retinitis pigmentosa.[ncbi.nlm.nih.gov] Abstract Usher syndrome type I is an autosomal recessive disease characterized by profound congenital hearing impairment and vestibular dysfunction followed by the onset of[ncbi.nlm.nih.gov] Abstract Usher syndrome type I (USH1), the most severe form of this syndrome, is characterized by profound congenital sensorineural deafness, vestibular dysfunction, and retinitis[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1D

    Abstract Usher syndrome type I (USH1) is an autosomal recessive disorder characterized by congenital sensorineural hearing loss, vestibular dysfunction and visual impairment[ncbi.nlm.nih.gov] Usher syndrome type 1 (USH1), with additional vestibular dysfunction, represents the most severe form and shows extensive allelic and non-allelic heterogeneity.[ncbi.nlm.nih.gov] Vestibular dysfunction manifests clinically as a delay in motor development. A key point is that walking age is often delayed ( 18 months).[umd.be]

  • Usher Syndrome

    dysfunction.[ncbi.nlm.nih.gov] Three clinical subtypes (USH1-USH3) are defined according to the severity of the hearing impairment, the presence or absence of vestibular dysfunction and the age of onset[ncbi.nlm.nih.gov] Usher syndrome (USH) is a clinically common autosomal recessive disorder characterized by retinitis pigmentosa (RP) and sensorineural hearing loss with or without vestibular[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1J

    Those with Usher syndrome type 2 do not have a dysfunctional vestibular system.[ushermom.com] Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction.[usherkidsaustralia.com] There is a prevalence of vestibular dysfunction in these patients.[audiologyonline.com]

  • Familial Progressive Vestibulocochlear Dysfunction

    Peripheral vestibular dysfunction can be caused by inner ear disorders, drug toxicity, neuritis, or a number of other causes.[clinicaltrials.gov] Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic sensorineural deafness with vestibular dysfunction.[doi.org] Those with Usher syndrome type 2 do not have a dysfunctional vestibular system.[usherkidsaustralia.com]

  • Meniere's Disease

    Cases 1 and 2 illustrate treatment of vertigo attacks caused by vestibular dysfunction in deaf ears.[ncbi.nlm.nih.gov] Patients with MD undergoing CI only may experience vestibular dysfunction which may cause long-term concerns.[ncbi.nlm.nih.gov] dysfunction.[ncbi.nlm.nih.gov]

  • Idiopathic Bilateral Vestibulopathy

    Effect of severity of vestibular dysfunction on postural instability in idiopathic bilateral vestibulopathy.[wwww.unboundmedicine.com] Results: By caloric test, most of the ITV patients had no vestibular dysfunction whereas the majority of the VN patients had severe vestibular dysfunction.[alliedacademies.org] […] bilateral vestibular dysfunction.[medlink.com]

  • Usher Syndrome Type 3B

    Those with Usher syndrome type 2 do not have a dysfunctional vestibular system.[ushermom.com] Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction.[usherkidsaustralia.com] Usher syndrome type III is characterized by postlingual, progressive hearing loss, variable vestibular dysfunction, and onset of retinitis pigmentosa symptoms, including nyctalopia[ncbi.nlm.nih.gov]

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