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375 Possible Causes for Cerebellar Ataxia, Progressive Loss of Vision, Spastic Paralysis

  • Infantile Neuronal Ceroid Lipofuscinosis

    We suggest CLN genes should be considered in the molecular analyses of patients presenting with adult-onset autosomal recessive cerebellar ataxia.[ncbi.nlm.nih.gov] […] degeneration of movement 0002333 Myoclonus 0001336 Progressive visual loss Progressive loss of vision Progressive vision loss Progressive visual impairment Slowly progressive[rarediseases.info.nih.gov] [icd10data.com] Cerebellar Ataxia We suggest CLN genes should be considered in the molecular analyses of patients presenting with adult-onset autosomal recessive cerebellar[symptoma.com]

  • Creutzfeldt Jakob Disease

    Common first symptoms are dementia, cerebellar ataxia, visual disturbance, and psychiatric symptoms. Seizure as the first symptom of CJD is a very rare finding.[ncbi.nlm.nih.gov] Symptoms of CJD Symptoms of CJD include: loss of intellect and memory changes in personality loss of balance and co-ordination slurred speech vision problems and blindness[nhs.uk] We report the case of an 18-year-old woman presented with cerebellar ataxia, blurred vision, rapidly progressive dementia, tremor and involuntary movements, urinary incontinence[ncbi.nlm.nih.gov]

  • Boucher-Neuhäuser Syndrome

    paralysis, infantile onset ascending (IAHSP) Spastic paraplegia, autosomal dominant Spastic paraplegia, autosomal recessive Spastic quadriplegic cerebral palsy Spinal muscular[genomediagnosticsnijmegen.nl] We describe two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia, Boucher-Neuhäuser syndrome, a rare but distinct pleiotropic single[ncbi.nlm.nih.gov] Progressive loss of vision, dyschromatopsia, and photophobia are the primary ocular symptoms. Night blindness and constricted visual fields are noted by some patients.[disorders.eyes.arizona.edu]

  • Spastic Paraplegia

    A wide variety of insults to the corticospinal tract result in spastic paralysis . The hereditary spastic paraplegias (HSPs) are single gene disorders in which...[link.springer.com] G11.0 Congenital nonprogressive ataxia G11.1 Early-onset cerebellar ataxia G11.2 Late-onset cerebellar ataxia G11.3 Cerebellar ataxia with defective DNA repair G11.4 Hereditary[icd10data.com] Progressive psychomotor regression can be seen.Weakness, loss of vision, and intellectual regression can recognized in some affected individuals.[5].[explainmedicine.com]

  • Hereditary Spastic Paraplegia

    KEYWORDS: ALS2; alsin; amyotrophic lateral sclerosis; infantile-onset ascending hereditary spastic paralysis (IAHSP)[ncbi.nlm.nih.gov] G11.0 Congenital nonprogressive ataxia G11.1 Early-onset cerebellar ataxia G11.2 Late-onset cerebellar ataxia G11.3 Cerebellar ataxia with defective DNA repair G11.4 Hereditary[icd10data.com] Progressive psychomotor regression can be seen.Weakness, loss of vision, and intellectual regression can recognized in some affected individuals.[5].[explainmedicine.com]

  • Neuronal Ceroid Lipofuscinosis

    paralysis Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness[csbg.cnb.csic.es] We suggest CLN genes should be considered in the molecular analyses of patients presenting with adult-onset autosomal recessive cerebellar ataxia.[ncbi.nlm.nih.gov] Most childhood forms of NCL are clinically characterized by progressive loss of vision as well as mental and motor deterioration, epileptic seizures, and premature death,[ncbi.nlm.nih.gov]

  • Alpers Syndrome

    Cerebellar ataxia develops in most patients. Peripheral neuropathy develops in many and becomes increasingly common in older children and young adults.[orpha.net] , called visual acuity Decrease in colour vision Progressive loss of central vision, eventually resulting in complete blindness Other symptoms Developing neurological features[lhsc.on.ca] ataxia in diseases classified elsewhere Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.[icd10data.com]

  • Chronic Alcoholism

    Abstract A 47-year-old chronic alcoholic with acute onset of spastic bulbar paralysis and quadriparesis with recovery has been reported.[ncbi.nlm.nih.gov] There was a progressive development of parkinsonism, cerebellar ataxia, and mental deterioration by the time he was 32.[ncbi.nlm.nih.gov] Such deleterious effect are possible if retinal ganglion cell loss related to chronic alcoholism (see below) progresses from preferential damage to P and K ganglion cells[scielo.br]

  • Autosomal Recessive Spastic Paraplegia Type 61

    Reid Published 2014 in Journal of Neurology DOI: 10.1007/s00415-014-7598-y The hereditary spastic paraplegias (HSPs) are a group of genetic conditions in which spastic paralysis[pdfs.semanticscholar.org] INTRODUCTION Autosomal recessive cerebellar ataxias (ARCA) constitute a subgroup of the hereditary cerebellar ataxias[ 1 ].[wjgnet.com] Ferraris S, Clark S, Garelli E, Davidzon G, Moore SA, et al. (2008) Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and[journals.plos.org]

  • Autosomal Recessive Spastic Paraplegia Type 56

    Reid Published 2014 in Journal of Neurology DOI: 10.1007/s00415-014-7598-y The hereditary spastic paraplegias (HSPs) are a group of genetic conditions in which spastic paralysis[pdfs.semanticscholar.org] "Autosomal dominant cerebellar ataxia type I Clinical features and MRI in families with SCA1, SCA2 and SCA" (PDF) .[en.wikipedia.org] Ferraris S, Clark S, Garelli E, Davidzon G, Moore SA, et al. (2008) Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and[journals.plos.org]

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