McCluskey D J, O'Connor P S, Sheehy J T
J Clin Neuroophthalmol. 1986 Jun;6(2):76-81.
The case of a patient with Charcot-Marie-Tooth disease who developed the acute fundus findings of Leber's optic neuropathy is described. Previous reports have proposed a genetic interrelationship between the two diseases. This relationship has been speculative, however, because the acute fundus findings of Leber's have never been observed in a case of Charcot-Marie-Tooth disease. This case adds support for a suggested genetic relationship between the two diseases. It is also possible that the optic atrophy previously described in Charcot-Marie-Tooth may represent the late findings of Leber's optic neuropathy.
本文描述了一例患有夏科-马里-图思病(Charcot-Marie-Tooth disease)的患者出现了莱伯遗传性视神经病变(Leber's optic neuropathy)的急性眼底表现。既往报道曾提出这两种疾病之间存在遗传相关性。然而,这种关系一直是推测性的,因为在夏科-马里-图思病患者中从未观察到莱伯遗传性视神经病变的急性眼底表现。该病例为这两种疾病之间存在遗传关系的推测提供了支持。也有可能,先前在夏科-马里-图思病中所描述的视神经萎缩可能代表莱伯遗传性视神经病变的晚期表现。