Hereditary ptosis of late onset: early observations on oculopharyngeal muscular dystrophy in Quebec by Roma Amyot

被引:1
|
作者
Duquette, P [1 ]
Giard, N [1 ]
机构
[1] HOP NOTRE DAME DE BON SECOURS, NEUROL SERV, MONTREAL, PQ H2L 4M1, CANADA
关键词
hereditary ptosis; oculopharyngeal muscular dystrophy (OPMD); French Canada; Roma Amyot;
D O I
10.1016/S0960-8966(97)00075-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In 1948, Roma Amyot, a well-known French-Canadian neurologist, observed in ten families a late onset syndrome consisting of hereditary ptosis which was sometimes associated with dysphagia but rarely with limb weakness. At that time, Taylor's original work dating back to 1915 was still unknown to him. Nonetheless, these reports constitute the two earliest publications about this syndrome prevalent in the French-Canadian population. Amyot recognized the myopathic nature of this disease which was later called oculopharyngeal muscular dystrophy (OPMD) by Victor et al. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:S12 / S14
页数:3
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