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Progressive cerebellar syndrome:- Case Discussion
1.
A 35 year
old man with progressive cerebellar syndrome and abnormal eye movements Submitted to AskTheNeurologist.Com in 2007 Author Anon.
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Cerebellar Ataxias Primary
Secondary Infectious Immune / inflammatory Toxic Metabolic / nutrional (acquired) Neoplastic Paraneoplastic Vascular Anatomical “ Sporadic” Inherited MSA-C “ apparently sporadic” Early onset < 20 years Late onset > 20 years Known metabolic defect FRDA EOCA with ret. Reflexes AT PME’s Mitochondrial ADCA’s (“SCA”) FRDA (occ. Late onset) DRPLA Mitochondrial FXTAS
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Cerebellar Ataxias Primary
Secondary Infectious Immune / inflammatory Toxic Metabolic / nutrional (acquired) Neoplastic Paraneoplastic Vascular Anatomical “ Sporadic” Inherited MSA-C “ apparently sporadic” Early onset < 20 years Late onset > 20 years Known metabolic defect FRDA EOCA with ret. Reflexes AT PME’s Mitochondrial ADCA’s (“SCA”) FRDA (occ. Late onset) DRPLA Mitochondrial FXTAS
32.
33.
Cerebellar Ataxias Primary
Secondary Infectious Immune / inflammatory Toxic Metabolic / nutrional (acquired) Neoplastic Paraneoplastic Vascular Anatomical “ Sporadic” Inherited MSA-C “ apparently sporadic” Early onset < 20 years Late onset > 20 years Known metabolic defect FRDA EOCA with ret. Reflexes AT PME’s Mitochondrial ADCA’s (“SCA”) FRDA (occ. Late onset) DRPLA Mitochondrial FXTAS
34.
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Cerebellar Ataxias Primary
Secondary Infectious Immune / inflammatory Toxic Metabolic / nutrional (acquired) Neoplastic Paraneoplastic Vascular Anatomical “ Sporadic” Inherited MSA-C “ apparently sporadic” Early onset < 20 years Late onset > 20 years Known metabolic defect FRDA EOCA with ret. Reflexes AT PME’s Mitochondrial ADCA’s (“SCA”) FRDA (occ. Late onset) DRPLA Mitochondrial FXTAS
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Submitted to
AskTheNeurologist.Com in 2007 Author Anon.