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13 Possible Causes for Appendicular Ataxia, Dysdiadochokinesis, Mutation in the WWOX Gene

  • Autosomal Recessive Spinocerebellar Ataxia 8

    Examination was notable for moderate dysarthria, hypermetric saccades and axial appendicular ataxia.[mdsabstracts.org] 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]

  • Spinocerebellar Ataxia Type 12

    30 See the list below: Clinical features Age of onset - 42-76 years (mean is 52 y) Relatively pure, slowly progressing gait and appendicular ataxia Dysarthria Lower limb[emedicine.medscape.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]

  • Spinocerebellar Ataxia Type 13

    Symptoms progress slowly; appendicular ataxia, dysmetria, dysdiadochokinesia, and cerebellar or mixed dysarthria (cerebellar and bulbar) appear at later stages. 14–16,22,23[elsevier.es] 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]

  • Ataxia

    One important distinction is between truncal ataxia and appendicular ataxia.[neuroexam.com] 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]

  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    […] progressive over weeks to months and stabilized within 6 months • The majority had both truncal and appendicular ataxia Brain (2003), 126, 1409 1418 66.[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]

  • Cerebellar Disease

    […] in the impairment of both appendicular and axial motor control.[movementdisorders.org] 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]

  • Autosomal Recessive Spinocerebellar Ataxia

    30 See the list below: Clinical features Age of onset - 42-76 years (mean is 52 y) Relatively pure, slowly progressing gait and appendicular ataxia Dysarthria Lower limb[emedicine.medscape.com] WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.[genome.jp] This deficit is most apparent in the execution of rapidly alternating movements, referred as dysdiadochokinesis by Babinski.[jpgmonline.com]

  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    30 See the list below: Clinical features Age of onset - 42-76 years (mean is 52 y) Relatively pure, slowly progressing gait and appendicular ataxia Dysarthria Lower limb[emedicine.medscape.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] Leukoencephalopathy Urinary urgency Spastic dysarthria Spastic ataxia Mild hearing impairment Ranula Scoliosis Retinal degeneration Progressive visual loss Inability to walk Dysdiadochokinesis[mendelian.co]

  • Autosomal Recessive Spastic Paraplegia Type 48

    Development Patients with ataxia Clinical history can be used to profile the onset and progression of the condition (progressive, non-progressive, or episodic ataxia), the[elsevier.es] 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] Gait was spastic–ataxic, and he had dysdiadochokinesis in both hands. Strength, coordination, and sensation were normal on bedside examination.[ng.neurology.org]

  • Autosomal Recessive Spastic Paraplegia Type 14

    Development Patients with ataxia Clinical history can be used to profile the onset and progression of the condition (progressive, non-progressive, or episodic ataxia), the[elsevier.es] 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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