Neurologic manifestations are rarely described in hereditary hemochromatosis (HH). We describe three patients with HH and movement disorders. Patient 1, a 69-year-old man, had a 13-year history of disabling cerebellar syndrome, action tremor and myoclonus, and secondary dementia. Patient 2 was a 40-
β¦ LIBER β¦
Transferrin sialic acid contents of patients with hereditary hemochromatosis
β Scribed by Min-Fu Tsan; Ursula Scheffel
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 400 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0361-8609
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