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过氧化物酶体双功能酶复合物缺乏症伴相关视网膜表现。

Peroxisomal bifunctional enzyme complex deficiency with associated retinal findings.

作者信息

Eustis H S, Curry T, Superneau D W

机构信息

Department of Ophthalmology, Ochsner Clinic, New Orleans, LA 70121, USA.

出版信息

J Pediatr Ophthalmol Strabismus. 1995 Mar-Apr;32(2):125-7. doi: 10.3928/0191-3913-19950301-16.

Abstract

Peroxisomal bifunctional enzyme complex deficiency is a recently recognized abnormality of fatty acid metabolism. We herein present the association of a flecked retina with peroxisomal bifunctional enzyme deficiency, a clinical association not previously reported. We suggest the finding of a flecked retina in an infant presenting with hypotonia, seizures, and failure to thrive is highly suggestive of this diagnosis.

摘要

过氧化物酶体双功能酶复合物缺乏是一种最近才被认识到的脂肪酸代谢异常。我们在此报告了斑点状视网膜与过氧化物酶体双功能酶缺乏之间的关联,这是一种此前未被报道的临床关联。我们认为,在出现肌张力减退、癫痫发作和发育不良的婴儿中发现斑点状视网膜强烈提示这一诊断。

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