Late Onset Optic Neuropathy in Methylmalonic and Propionic Acidemia

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• 作者：Zoë ; R. Williams ; P. Emmett Hurley ; Ugur E. Altiparmak ; Steven E. Feldon ; Georgianne L. Arnold ; Eric Eggenberger ; Luis J. Mejico
• 刊名：American Journal of Ophthalmology
• 出版年：2009
• 出版时间：May 2009
• 年：2009
• 卷：147
• 期：5
• 页码：929-933
• 全文大小：240 K

文摘

Purpose

To describe 3 cases of late-onset bilateral optic neuropathy with visual dysfunction in patients with organic acidemia.

Design

Retrospective case series.

Methods

A total of 3 subjects, a 16-year-old male with methylmalonic acidemia (MMA), a 21-year-old male with MMA, and a 20-year-old female with propionic acidemia (PA), are included in this series. Comparison of the patients' clinical course, ophthalmologic exam, and testing are discussed. The outcome measures include visual acuity (VA), fundus appearance, visual fields, brain imaging, and genetic testing.

Results

All 3 subjects had late-onset severe bilateral VA loss with bilateral optic nerve pallor, central or cecocentral scotomas on visual field testing, and negative diagnostic workups for other causes of bilateral optic neuropathy.

Conclusions

Patients with organic acidemia may develop late-onset bilateral optic neuropathy with visual dysfunction despite lifelong propiogenic amino acid restriction and dietary supplementation.