Routsonis K, Georgiadis G
J Neurol Sci. 1984 May;64(2):161-73. doi: 10.1016/0022-510x(84)90034-0.
Seven members in three generations of a family are affected with peroneal muscular atrophy. Five have the disorder in combination with epilepsy. The proposita exhibits a cerebellar syndrome, she and one brother show choreiform movements, and she, her mother and a great-uncle have pes cavus. One member has EEG abnormalities but no muscular atrophy. The familial occurrence of this combination of symptoms has not been described before. In this family the syndrome is transmitted as an autosomal dominant with variable expressivity.
一个家族三代中的七名成员患有腓骨肌萎缩症。其中五人同时患有该疾病和癫痫。先证者表现出小脑综合征,她和一个兄弟有舞蹈样动作,她、她的母亲和一位叔祖父有高弓足。一名家族成员有脑电图异常但无肌肉萎缩。这种症状组合的家族性发生情况此前尚未有过描述。在这个家族中,该综合征以具有可变表达性的常染色体显性方式遗传。