2021
DOI: 10.1002/mdc3.13285
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Uremic Striatopallidal Syndrome Manifesting as Acute Onset Chorea

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Cited by 2 publications
(2 citation statements)
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“…We were unable to establish a definite cause of chorea in 8 cases (cases [31][32][33][34][35][36][37][38], despite an extensive work-up. We suspected frontotemporal dementia in 4 cases (cases 30, 33,34 and 37) and hereditary ataxia in 2 patient (case 32 and 36) although the findings of genetic analyses were negative for hexanucleotide expansion (C9ORF72), progranulin mutation and/or common dominant hereditary/recessive ataxias (SCA 1,2-3-6,7,8, 17,36, DRPLA and Friedreich).…”
Section: Unknown Etiologymentioning
confidence: 88%
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“…We were unable to establish a definite cause of chorea in 8 cases (cases [31][32][33][34][35][36][37][38], despite an extensive work-up. We suspected frontotemporal dementia in 4 cases (cases 30, 33,34 and 37) and hereditary ataxia in 2 patient (case 32 and 36) although the findings of genetic analyses were negative for hexanucleotide expansion (C9ORF72), progranulin mutation and/or common dominant hereditary/recessive ataxias (SCA 1,2-3-6,7,8, 17,36, DRPLA and Friedreich).…”
Section: Unknown Etiologymentioning
confidence: 88%
“…Chorea may be observed in many systemic and metabolic conditions such as uncontrolled diabetes, liver and renal disease, hyperthyroidism, electrolyte disturbances and vitamin B12 deficiency [8,10,[32][33][34][35][36][37][38]. Suspicion of metabolic disorders can be especially high when movement disorders, including chorea, are observed in emergency settings [8,10].…”
Section: Discussionmentioning
confidence: 99%