Delayed diagnosis of ataxia with oculomotor apraxia type 2 in a Peruvian patient, a case report
Delayed diagnosis of ataxia with oculomotor apraxia type 2 in a Peruvian patient, a case report
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Netherlands: Elsevier B.V
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English
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Netherlands: Elsevier B.V
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AbstractIntroductionAtaxia with oculomotor apraxia type 2 (AOA2) is a rare autosomal recessive cerebellar ataxia characterized by progressive cerebellar ataxia, sensorimotor peripheral neuropathy, and occasional oculomotor apraxia. Case reportA 50-year-old male with a history of orthopedic shoe use since childhood presented with slowly progressive...
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Delayed diagnosis of ataxia with oculomotor apraxia type 2 in a Peruvian patient, a case report
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TN_cdi_proquest_miscellaneous_3176341633
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3176341633
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0303-8467,1872-6968
E-ISSN
1872-6968
DOI
10.1016/j.clineuro.2025.108823
