A family with hereditary amyloidosis characterized by peripheral neuropathy and cardiomyopathy is described. Lack of eye involvement sets their disease apart from the Indiana/Swiss familial amyloidotic polyneuropathy type 11. The disease is of late onset; affected members die of cardiomyopathy after
A kindred of hereditary adult-onset leukodystrophy with sparing of the optic radiations
β Scribed by K. Abe; M. Ikeda; K. Watase; H. Tanabe; H. Fujimura; S. Yorifuji; S. Ueno; T. Mezaki; T. Mori
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 620 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0028-3940
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