Table7.
Therapeutic Interventions for Cerebellar Ataxia | ||
---|---|---|
Targeted disease-modifying therapy for acquired disorders | Wernicke encephalopathy & chronic alcohol use Immune-mediated Paraneoplastic Gluten-associated ataxia |
Thiamine, 1500 mg, IV daily × 2 d then 250 mg daily × 5 d Thiamine, 100 mg, PO daily Methylprednisolone, 1000 mg, IV × 3–5 d ± IVIG Methylprednisolone, 1000 mg, IV × 5 d + IVIG/plasmapheresis Gluten-free diet |
Targeted disease-modifying therapy for inherited disorders | Niemann-Pick type C Abetalipoproteinemia GLUT-1 deficiency Cerebrotendinous xanthomatosis |
Miglustat 200 mg TID Vitamin E, 150 mg/kg/d Ketogenic diet, avoid fasting Chenodeoxycholic acid, 250 mg, TID |
Symptomatic therapy | Cerebellar ataxia SCA3 Episodic ataxia type 1 Episodic ataxia type 2 |
Riluzole, 50 mg, BID Varenicline, 1 mg, BID Carbamazepine Acetazolamide, 250–1000 mg/d, 4-aminopyridine, 15 mg/d |
Abbreviations: BID, twice daily; d, day(s); GLUT, glucose transporter; IV, intravenous; IVIG, intravenous immunoglobulins; kg, kilograms; mg, milligrams; TID, three times per day.