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3,097 Possible Causes for Arrhythmias Detected Prenatally, Autofluorescent Lipopigment in Neurons, Cerebellar Ataxia

  • Infantile Neuronal Ceroid Lipofuscinosis

    […] by an accumulation of autofluorescent lipopigments in neurons and extraneuronal tissues.[alliedacademies.org] 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] Synonyms Batten disease, Kuf disease Symtoms and course NCL are characterised by psychomotor deterioriation, visual failure, and the accumulation of autofluorescent lipopigment[alzheimer-europe.org]

    Missing: Arrhythmias Detected Prenatally
  • Neuronal Ceroid Lipofuscinosis

    Neuronal ceroid lipofuscinoses are a group of rare neurodegenerative disorders that are characterised by an accumulation of autofluorescent lipopigments in neurons and extraneuronal[ncbi.nlm.nih.gov] 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] , epilepsy and the accumulation of an autofluorescent lipopigment in neurones and other cells.[ncbi.nlm.nih.gov]

    Missing: Arrhythmias Detected Prenatally
  • Progressive Myoclonic Epilepsy Type 3

    Neuronal Ceroid Lipofuscinosis  autosomal recessive disease.  characterized by progressive myoclonus with visual failure and accumulation of an autofluorescent lipopigment[slideshare.net] Clinical manifestations of the patients include cerebellar ataxia with myopathy, recurrent headache, and myoclonus and epilepsy....[connection.ebscohost.com] ataxia, dementia, and progression of the disease.[scholar.sun.ac.za]

    Missing: Arrhythmias Detected Prenatally
  • Northern Epilepsy

    autofluorescent lipopigment 0002074 Myoclonus 0001336 Seizures Seizure 0001250 Showing of 19 Last updated: 12/1/2018 Making a diagnosis for a genetic or rare disease can[rarediseases.info.nih.gov] These occur in approximately 50-70% of individuals with TSC, and are most frequently detected prenatally or in the neonatal period.[clinicaladvisor.com] Cerebellar Ataxia Type 1, Autosomal Dominant Cerebellar Ataxia, Ataxia-telangiectasia-like Disorder, Ataxia-intellectual Disability-oculomotor Apraxia-cerebellar Cysts Syndrome[crm.diseaseinfosearch.org]

  • Progressive Myoclonic Epilepsy Type 7

    Neuronal Ceroid Lipofuscinosis  autosomal recessive disease.  characterized by progressive myoclonus with visual failure and accumulation of an autofluorescent lipopigment[slideshare.net] ataxia Autosomal dominant cerebellar ataxia type I Autosomal dominant cerebellar ataxia type II Autosomal dominant cerebellar ataxia type III Autosomal dominant cerebellar[se-atlas.de] In advanced cases, inability to coordinate voluntary muscle movements (cerebellar ataxia) occurs.[rarediseases.org]

    Missing: Arrhythmias Detected Prenatally
  • MERRF Syndrome

    lipopigment in the neurons and glial elements. [33] , [34] The first report of NCL from India was a patient with juvenile onset NCL by Gulati et al., [13] subsequently we[bioline.org.br] Abstract Myoclonic epilepsy and ragged-red fibers (MERRF) syndrome is a rare disorder characterized by myoclonus, muscle weakness, cerebellar ataxia, heart conduction block[ncbi.nlm.nih.gov] There may also be seizures, cerebellar ataxia and myopathy.[en.wikipedia.org]

    Missing: Arrhythmias Detected Prenatally
  • Hereditary Spastic Paraplegia

    […] ceroid lipofuscinosis (#606693), a neurodegenerative disorder characterized by the intracellular accumulation of autofluorescent lipopigments.[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] […] following cerebrovascular disease ( I69. with final characters -93) hereditary G11.9 ICD-10-CM Diagnosis Code G11.9 Hereditary ataxia, unspecified 2016 2017 2018 2019 Billable[icd10data.com]

    Missing: Arrhythmias Detected Prenatally
  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    […] disorders characterized by the intracellular accumulation of autofluorescent lipopigment storage material in different patterns ultrastructurally.[mendelian.co] MalaCards based summary : Spastic Ataxia 3, Autosomal Recessive, is also known as ataxia, spastic, 3, autosomal recessive, and has symptoms including gait ataxia, cerebellar[malacards.org] […] intracellular accumulation of autofluorescent lipopigment storage material in different patterns ultrastructurally.[mendelian.co]

    Missing: Arrhythmias Detected Prenatally
  • Unverricht-Lundborg Syndrome

    Neuronal Ceroid Lipofuscinosis  autosomal recessive disease.  characterized by progressive myoclonus with visual failure and accumulation of an autofluorescent lipopigment[slideshare.net] Read More About Neuroimmunology & Neuroinflammation Clinical Reasoning: Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy ... decline, neuropathy[aan.com] MD Neurology February 24, 2004 An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures ...- Unverricht - Lundborg disease mapping[aan.com]

    Missing: Arrhythmias Detected Prenatally
  • Chronic Alcoholism

    There was a progressive development of parkinsonism, cerebellar ataxia, and mental deterioration by the time he was 32.[ncbi.nlm.nih.gov] Others develop for non-hereditary reasons, such as alcoholic cerebellar ataxia. What Is Cerebellar Ataxia? Cerebellar ataxia is a symptom, not a distinct disorder.[promises.com] * Affects nearly every organ system: NEURO – Affects both peripheral nervous system (peripheral neuropathy) and central nervous sytem : Cognitive dysfunction, Cerebellar degeneration[errolozdalga.com]

    Missing: Arrhythmias Detected Prenatally Autofluorescent Lipopigment in Neurons

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