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The nanophthalmic macula

机译:纳米眼科黄斑

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摘要

AIMS—To define an unusual macular appearance found in association with nanophthalmos.
METHODS—A case review.
RESULTS—Seven children (aged 8 months to 17 years) with nanophthalmos were examined. They all exhibited the same clinical findings of an unusual yellow macula appearance with retinal folds and crowded optic discs. Visual electrophysiology performed in four cases was normal.
CONCLUSION—A distinctive yellow macular pigmentation with associated chorioretinal folds and crowded optic discs is present in nanophthalmos. It is proposed that the retinal folds are due to a disparity between scleral and retinal growth while the macula discoloration is due to a congenital abnormality in arrangement or position of the luteal pigment and is not degenerative. Included in this case series is the second case in the literature of nanophthalmos associated with Kenny's syndrome. Inheritance of nanophthalmos appears to be autosomal recessive.

Keywords: nanophthalmos; maculopathy; Kenny's syndrome
机译:目的-定义与纳米眼病有关的异常黄斑外观。
方法-病例回顾。
结果-检查了七名儿童(年龄8个月至17岁)。他们都表现出相同的临床发现,即出现异常的黄色黄斑,视网膜褶皱和拥挤的视盘。 4例患者的视觉电生理正常。
结论—纳米眼内存在明显的黄斑黄斑,伴有脉络膜视网膜褶皱和拥挤的视盘。提出视网膜褶皱是由于巩膜和视网膜生长之间的差异而引起的,而黄斑变色则是由于黄体色素的排列或位置的先天性异常而不是退化的。该病例系列中包括与肯尼综合症有关的纳米眼炎文献中的第二例。纳米眼的遗传似乎是常染色体隐性遗传。

关键词:纳米眼;黄斑病;肯尼综合症

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