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17 Possible Causes for Dizziness, Dysdiadochokinesis, Mutation in the WWOX Gene

  • Spinocerebellar Ataxia Type 12

    He is currently part of the Interdisciplinary Center for Vertigo & Balance Disorders at the University Hospital Zurich.[books.google.com] Mutation in the WWOX gene, D. schematic of the WWOX gene). Figure adapted from WWOX.[epilepsygenetics.net] MalaCards based summary : Spinocerebellar Ataxia 12, also known as sca12, is related to spinocerebellar ataxia 36 and aceruloplasminemia, and has symptoms including dysdiadochokinesis[malacards.org]

  • Cerebellar Disease

    […] cases should have urgent CT or MRI scan as surgical decompression is successful at the early stage. p Neoplastic Disorders Brainstem and cerebellar neoplasm can lead to dizziness[otologytextbook.net] WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.[genome.jp] Limb ataxia is shown by limbs that are clumsy, discoordinated, and that have difficulty with rapidly alternating movements (a phenomenon unhelpfully known as dysdiadochokinesis[medicguide.blogspot.com]

  • Ataxia

    Patient 1 presented with dizziness and acute yet mild limb and gait ataxia.[ncbi.nlm.nih.gov] The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.[ncbi.nlm.nih.gov] Nystagmus; Vestibulo-ocular reflex (VOR) Postural and gait dysfunction Midline (Vermis; paleocerebellum)Truncal & gait ataxia Hemisphere (Neocerebellum)Limb ataxia: Dysmetria, Dysdiadochokinesis[neuromuscular.wustl.edu]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    , or dizziness Continued Causes of Ataxia Around 150,000 people in the U.S. deal with some form of ataxia.[webmd.com] Mutation in the WWOX gene, D. schematic of the WWOX gene). Figure adapted from WWOX.[epilepsygenetics.net] […] hemisphere) Neocerebellum Connected with Pons and cortex through thalalmus Planning and initiation of movements Regulation of fine limb movements Limb ataxia: Dysmetria, Dysdiadochokinesis[slideshare.net]

  • Autosomal Recessive Spinocerebellar Ataxia

    , or dizziness Continued Causes of Ataxia Around 150,000 people in the U.S. deal with some form of ataxia.[webmd.com] WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.[genome.jp] 29 See the list below: Clinical features Nonprogressive ataxia Nystagmus Dysarthria Psychomotor display Clumsiness Cognitive impairment Frequent falling early in disease Dysdiadochokinesis[emedicine.medscape.com]

  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    In Children History:  refusal to walk or with a wide-based, "drunken" gait.  Vertigo, dizziness and vomiting  Personality and behavioral changes.  Abnormal mental status[slideshare.net] The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. Brain. 2014;137:411–9.[cerebellumandataxias.biomedcentral.com] 29 See the list below: Clinical features Nonprogressive ataxia Nystagmus Dysarthria Psychomotor display Clumsiness Cognitive impairment Frequent falling early in disease Dysdiadochokinesis[emedicine.medscape.com]

  • Myelocerebellar Disorder

    Delusion Dementia Diabetic Neuropathy Diabetic Polyneuropathy Diplopia Discitis Discogenic Pain Distal Muscle Weakness Distal Myopathy Distal Myopathy With Vocal Cord Weakness Dizziness[healthgrades.com] WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.[genome.jp] […] hemisphere) Neocerebellum Connected with Pons and cortex through thalalmus Planning and initiation of movements Regulation of fine limb movements Limb ataxia: Dysmetria, Dysdiadochokinesis[slideshare.net]

  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    EA2 Unknown 3-52 Lifelong Nystagmus; attacks last minutes to hours; posture change induced; vertigo; later permanent ataxia 63.[slideshare.net] Koenig, The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. Brain, 2014. 137(Pt 2): p. 411-9.[hih-tuebingen.de] Leukoencephalopathy Urinary urgency Spastic dysarthria Spastic ataxia Mild hearing impairment Ranula Scoliosis Retinal degeneration Progressive visual loss Inability to walk Dysdiadochokinesis[mendelian.co]

  • Spinocerebellar Ataxia Type 13

    Double vision, dysarthria, impaired hand writing, and episodic vertigo preceded ataxia in 4% of patients, respectively.[real.mtak.hu] WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.[genome.jp] The neurologic examination showed markedly slow ocular saccades, dysarthria, upper and lower limb dysmetria, dysdiadochokinesis, and wide-based ataxic gait.[jamanetwork.com]

  • Autosomal Recessive Spastic Paraplegia Type 49

    Migrainous Vertigo Migrainous vertigo is a term used to describe episodic vertigo in patients with a history of migraines or with other clinical features of migraine.[aetna.com] Koenig, The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. Brain, 2014. 137(Pt 2): p. 411-9.[hih-tuebingen.de] The patient developed dysdiadochokinesis, but no cerebellar ocular signs were noted.[omicsonline.org]

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