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5,103 Possible Causes for Arrhythmias Detected Prenatally, Autofluorescent Lipopigment in Neurons, Rapid Progression

  • Neuronal Ceroid Lipofuscinosis Type 4B

    […] deterioration of vision and a slower, but progressive deterioration of intellect.[patient.info] […] of autofluorescent lipopigment storage material 0003208 Granular osmiophilic deposits (GROD) in cells 0003657 Increased neuronal autofluorescent lipopigment 0002074 Myoclonus[rarediseases.info.nih.gov] […] clinically and genetically heterogeneous group of neurodegenerative disorders characterized by the intracellular accumulation of autofluorescent lipopigment storage material[humpath.com]

    Missing: Arrhythmias Detected Prenatally
  • Late-Infantile Neuronal Ceroid Lipofuscinosis

    The infantile form has the most rapid progression and children live into their mid childhood years.[drewshope.com] 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] The infantile form has the most rapid progression and children live into their mid-childhood years.[noahshope.com]

    Missing: Arrhythmias Detected Prenatally
  • Neuronal Ceroid Lipofuscinosis

    progression of neurodegeneration, is due to CLN2 gene mutations.[ncbi.nlm.nih.gov] 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] , epilepsy and the accumulation of an autofluorescent lipopigment in neurones and other cells.[ncbi.nlm.nih.gov]

    Missing: Arrhythmias Detected Prenatally
  • Infantile Neuronal Ceroid Lipofuscinosis

    The infantile form has the most rapid progression and children live into their mid childhood years.[katwasabi.com] […] by an accumulation of autofluorescent lipopigments in neurons and extraneuronal tissues.[alliedacademies.org] Patient 6, however, presented an atypical progression of disease.[scielo.br]

    Missing: Arrhythmias Detected Prenatally
  • Adult Neuronal Ceroid Lipofuscinosis

    The infantile form has the most rapid progression and children live into their mid childhood years.[brainfoundation.org.au] A unifying feature of these devastating conditions is the lysosomal accumulation of autofluorescent lipopigment in neuronal cells [1], [2].[journals.plos.org] […] accumulation of autofluorescent lipopigments.[jnnp.bmj.com]

    Missing: Arrhythmias Detected Prenatally
  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    Disease progression was rapid, and the majority of patients died from respiratory failure within 1–5 years after onset of disease.[link.springer.com] Hereditary pure lower motor neuron disease with adult onset and rapid progression. J Neurol 2001 ; 248 : 290 –96.[academic.oup.com] Wokke Abstract We describe three members each of two families presenting with a hereditary form of lower motor neuron disease with adult onset and rapid progression and compare[link.springer.com]

    Missing: Arrhythmias Detected Prenatally Autofluorescent Lipopigment in Neurons
  • Neuronal Ceroid Lipofuscinosis Type 8

    Patient 6, however, presented an atypical progression of disease.[scielo.br] […] processes: accumulation of autofluorescent lipopigments within various cell types and loss of cells, especially in the cerebral cortex1- 3.[elyzeyiko.gq] Despite the early-developing symptoms, rapid evolution to a difficult-to-treat myoclonic epilepsy and blindness, this patient was alive at the age of 19 years, although in[scielo.br]

    Missing: Arrhythmias Detected Prenatally
  • Neuronal Ceroid Lipofuscinosis Type 10

    Patient 6, however, presented an atypical progression of disease.[scielo.br] […] processes: accumulation of autofluorescent lipopigments within various cell types and loss of cells, especially in the cerebral cortex 1-3 .[scielo.br] Despite the early-developing symptoms, rapid evolution to a difficult-to-treat myoclonic epilepsy and blindness, this patient was alive at the age of 19 years, although in[scielo.br]

    Missing: Arrhythmias Detected Prenatally
  • Congenital Neuronal Ceroid Lipofuscinosis 

    Over time, progressive MPS deposition in the brain leads to seizures in 60–70%, spasticity, and feeding difficulties.[ncbi.nlm.nih.gov] […] material containing autofluorescent lipopigments.[ncbi.nlm.nih.gov] Those with severe disease undergo rapid regression with loss of 9–15 developmental quotient (DQ) points per year ( 12 ).[ncbi.nlm.nih.gov]

    Missing: Arrhythmias Detected Prenatally
  • Neuronal Ceroid Lipofuscinosis Type 3

    Ocularly, Batten disease is characterized by a rapid deterioration of vision, progressing to blindness within a few years.[ncbi.nlm.nih.gov] […] by an accumulation of autofluorescent lipopigments in neurons and extraneuronal tissues.[alliedacademies.org] The infantile form has the most rapid progression and children live into their mid childhood years.[brainfoundation.org.au]

    Missing: Arrhythmias Detected Prenatally

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