Yonsei Med J.  1988 Sep;29(3):233-238. 10.3349/ymj.1988.29.3.233.

Olivopontocerebellar Atrophy

• Choi IS
• Lee MS
• Kim WT
• Choi KK

• KMID: 1729552
• DOI: http://doi.org/10.3349/ymj.1988.29.3.233

Abstract

Between 1985and 1987, 31 patients with sporadic olivopontocerebellar atrophy (SOPCA) and 3 patients with familial olivopontocerebellar atrophy (FOPCA) were examined in the Neurologic Clinic of Yongdong Severance Hospital. The incidence of the disease among our neurology clinic patients was 0.9% and 3.4% of those patients were admitted. Seventeen of them were men and seventeen women, and their ages of onset ranged from 16 to 75 years (mean, 48.2 years). In comparison with SOPCA, the disease began earlier in FOPCA (mean age, 51.0 VS 19.3 years), but there were no other differences in clinical feature of the disease. Four patients had parkinsonism, one dementia, and one ophthalmoplegia. None presented spinal involvement or abnormal movements. Eight had a coexisting disease; 3, ch(03)nic alcoholism; 2, hypertension; 2, diabetes mellitus; and 1, malignant neoplasm.

Keyword

Olivopontocerebellar atrophy; FOPCA; SOPCA

MeSH Terms

Adolescent
Adult
Aged
Diagnosis, Differential
Female
Human
Korea
Male
Middle Age
Olivopontocerebellar Atrophies/*diagnosis/epidemiology/genetics
Spinocerebellar Degenerations/*diagnosis