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Dimitrios Kalogeropoulos1, Lilia Lagha1, Andrew J Lotery1,2

  • 1Southampton Eye Unit, University Hospital Southampton, Southampton, United Kingdom; and.

PubMed
概括

阿尔法-甲基-CoA赛马酶缺乏症是一种罕见的遗传疾病,在一个患有无症状视网膜功能障碍的年轻女性患者中被发现. 这一案例凸显了视网膜衰变和各种系统性表现的潜力,即使在无症状个体中也是如此.

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