Lewkonia R M, Buxton P H
J Neurol Neurosurg Psychiatry. 1973 Oct;36(5):820-5. doi: 10.1136/jnnp.36.5.820.
The occurrence of myositis in a father and his daughter is reported. The daughter's illness resembled childhood dermatomyositis and progressed to systemic involvement and death less than four years from the onset of symptoms. In the case of the father the illness followed the course of adult polymyositis and there was little evidence of systemic involvement. The immunological and genetic significance of the two cases is discussed.
本文报道了一位父亲及其女儿患肌炎的病例。女儿的病情类似儿童皮肌炎,症状出现后不到四年便进展为全身受累并死亡。父亲的病情则符合成人多发性肌炎的病程,几乎没有全身受累的迹象。文中讨论了这两个病例的免疫学及遗传学意义。