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.
机构:
Hull Royal Infirm, Dept Neurol, Kingston Upon Hull HU3 2JZ, N Humberside, EnglandHull Royal Infirm, Dept Neurol, Kingston Upon Hull HU3 2JZ, N Humberside, England
机构:
Univ New S Wales, St George Hosp, Dept Dermatol, Sydney, NSW, AustraliaRoyal Childrens Hosp Melbourne, Childrens Neurosci Ctr, Parkville, Vic 3052, Australia