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280:-pallidoluysian atrophy (DRPLA), brain iron accumulation disorders, Wilson's...
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148:-pallidoluysian atrophy: Clinical features and molecular genetics". Adv...
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degeneration: a clinicopathological study of the Ramsay Hunt syndrome"...
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controlling seizures and improving neurological dysfunction in a patient with
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pallidoluysian atrophy. Type I ADCA is characterized by different symptoms...
615:-pallidoluysian atrophy (DRPLA)". Epilepsy Behav Case Rep. 8: 44–46....
504:-pallidoluysian atrophy Dentin dysplasia sclerotic bones Dentin dysplasia...
471:–pallidoluysian atrophy Unverricht–Lundborg disease MERRF syndrome Lafora...
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Shaw, C. M. (February 1978). "Progressive myoclonus and epilepsy with
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dyssynergia cerebellaris myoclonica, dyssynergia cerebellaris progressiva,
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260–266. doi:10.1093/ageing/afp020. PMID 19276093. Tsuji, S. (1999). "
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674:-pallidoluysian atrophy. This encoded protein is characterized by two...
438:-pallidoluysian atrophy and neuroferritinopathy. Also, some autosomal...
412:-Pallidoluysian Atrophy DRT dead right there DS disease Down syndrome...
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Purkinje cells send their afferents to the ipsilateral dentate nucleus.
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contains a polyglutamine repeat, expansion of which is responsible for
556:–pallidoluysian atrophy ( trinucleotide expansion in the DRPLA gene)...
408:(DPT vaccine) DRE Digital Rectal ExaminationDilated Retinal Exam DRPLA
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disease and
Huntington disease-like 2, spinal-bulbar muscular atrophy,
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specific symptoms CAG Varies with type More often through father Exon
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system. This protein has also been identified as interacting with the
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degeneration, or Ramsay Hunt cerebellar syndrome. Onset of symptoms...
731:-pallidoluysian atrophy/Haw River syndrome Cerebellar atrophy, ataxia
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deficienciency Dental caries Dental fluorosis Dental tissue neoplasm
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status epilepticus
Myoclonic epilepsy Progressive myoclonus epilepsy
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Other autosomal dominant diseases that can be misdiagnosed as HD are
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