Emery A E
Medical School, University of Edinburgh, U.K.
Neuromuscul Disord. 1993 Jul;3(4):263-6. doi: 10.1016/0960-8966(93)90018-f.
In a communication to the Royal Medical and Chirurgical Society of London in December 1851, which was published in the Transactions of the Society the following year, Edward Meryon, an English physician, described, in considerable detail, eight boys in three families with a disease later referred to as Duchenne muscular dystrophy. He was particularly impressed by the predilection for males and its familial nature, and that the progressive muscle wasting and weakness was essentially due to a disease of muscle and not the nervous system. His detailed histological studies revealed no abnormality of the spinal cord or nerves but in muscle tissue he noted extensive "granular degeneration" and in particular that the sarcolemma was broken down and destroyed. He appears to have been the first physician to make a detailed clinical, genetic, and pathological study of the disorder several years before Duchenne.
1851年12月,英国医生爱德华·梅里昂在致伦敦皇家医学与外科学会的一封信中,相当详细地描述了三个家庭中的八个男孩患有一种后来被称为杜兴氏肌肉营养不良症的疾病。这封信于次年发表在该学会的《会刊》上。他对该病男性易患以及家族性特点印象深刻,还发现进行性肌肉萎缩和无力本质上是由肌肉疾病而非神经系统疾病导致的。他详细的组织学研究显示脊髓和神经没有异常,但在肌肉组织中,他注意到广泛的“颗粒变性”,特别是肌膜被破坏。他似乎是在杜兴之前几年就对这种疾病进行详细临床、遗传和病理学研究的首位医生。