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Rat Model of Photochemically-Induced Posterior Ischemic Optic Neuropathy
Published on: November 29, 2015
[Anterior ischemic optic neuropathy in children]
1División de Neurología Pediátrica, New York Presbyterian Hospital, NY 10021, USA.
Insights
A child on peritoneal dialysis developed sudden bilateral blindness due to anterior ischemic optic neuropathy. Prompt treatment did not restore vision, highlighting the severity of this condition in pediatric patients.
Area of Science:
- Ophthalmology
- Nephrology
- Pediatrics
Background:
- A 5-year-old girl with chronic renal failure from congenital kidney disease underwent peritoneal dialysis.
- She experienced asymptomatic arterial hypotension post-dialysis.
Observation:
- The patient presented with sudden, severe bilateral blindness, including absent light perception and unresponsive pupils.
- Ophthalmoscopy revealed pale optic discs and abnormal retinal vasculature.
- Neurological and MRI evaluations were unremarkable.
Findings:
- The final diagnosis was anterior ischemic optic neuropathy.
- Despite treatment with corticosteroids, antibiotics, and antivirals, vision loss was permanent.
Implications:
- This case underscores the risk of anterior ischemic optic neuropathy in children with chronic kidney disease and peritoneal dialysis.
- Early recognition and management are crucial, though outcomes can be poor.
- Further research into pathogenesis and preventative strategies is warranted.
Abstract:
A 5-year old girl with history of chronic renal failure due to dysplastic and polycystic kidney disease treated with peritoneal dialysis since birth wake up the the day after an scheduled uncomplicated peritoneal dialysis except for asymptomatic arterial hypotension with bilateral blindness. Neurological examination was normal except for absent light perception and tracking of optokinetic tape, dilated (7 mm) and unresponsive to light pupils, pale and slighted elevated disks with blurred margins and pale retina with irregular abnormal appearing vessels. Spinal fluid examination revealed no abnormalities except for slight pleocytosis (12 WBC, 68% mononuclears and 32% lymphocytes). MRI with gadollinium and MRA were normal. She received intravenous methyprednisolone for 3 days and intravenous and intraperitoneal antibiotics and intravenous acyclovir without improvement. She also received topical dorsolamide hydrochloride. Two year later she remained blind without light perception. Final diagnosis was anterior ischemic optic neuropathy. Pathogenesis, clinical picture, differential diagnosis and treatment of this condition in children are discussed.
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