Transient Cortical Blindness in a Toddler With Heterozygous Ornithine Transcarbamylase Deficiency-Reference-Cited by-同舟云学术

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Transient Cortical Blindness in a Toddler With Heterozygous Ornithine Transcarbamylase Deficiency

Published:2021-11-30 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Eskander Peter N,Romani Sara S

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference12 articles.

1. Urea cycle disorders overview;Mew NA,2003

2. Urea cycle disorders: diagnosis, pathophysiology, and therapy;Brusilow SW;Adv Pediatrics,1996

3. Protracted cortical visual loss in a child with ornithine transcarbamylase deficiency;Anderson JM;J Neuroophthalmol,2010

4. Ornithine transcarbamylase deficiency presenting with acute reversible cortical blindness;Prasun P;J Child Neurol,2015

5. Transient visual loss in ornithine transcarbamoylase deficiency;Snebold NG;Am J Ophthalmol,1987

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