Cataract surgery in Knobloch syndrome: a case report

被引：5

作者：

Bongiovanni, Carmen Slvia ^{[1
]}

Serra Ferreira, Carla Cristina ^{[1
]}

Silverio Rodrigues, Ana Paula ^{[1
]}

Fortes Filho, Joao Borges ^{[2
]}

Tartarella, Marcia Beatriz ^{[1
]}

机构：

[1] Univ Fed Sao Paulo, Med Sch, Dept Ophthalmol, Congenital Cataract Sect, Sao Paulo, Brazil

[2] Univ Fed Rio Grande do Sul, Med Sch, Dept Ophthalmol, Porto Alegre, RS, Brazil

来源：

CLINICAL OPHTHALMOLOGY | 2011年 / 5卷

关键词：

Knobloch syndrome; cataract; phacoemulsification; vitreous; right eye; left eye; genetic;

D O I：

10.2147/OPTH.S18989

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

Knobloch syndrome is an autosomal recessive disorder associated with early-onset ocular abnormalities and central nervous system malformations. Ocular abnormalities are usually severe, and include high myopia, vitreoretinal degeneration, retinal detachment, macular abnormalities, and cataract. The most frequent systemic changes are midline malformations of the brain, ventricular dilation, and occipital encephalocele. Cognitive delay may occur. We report a case of cataract in a child with Knobloch syndrome. Cataract surgery and follow-up are described.

引用

页码：735 / 737

页数：3

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