Optic neuropathy from hypovitaminosis A in a series of children with severe dietary restrictions

Author:

Shi Jane12,Caldwell James3,Sheck Leo12,Tsang Bobby14,Alekzander Rebecca5,Escardo‐Paton Julia2,Vincent Andrea L12,Spooner Claire6,Heppner Peter17,Danesh‐Meyer Helen12,Hull Sarah12ORCID

Affiliation:

1. Faculty of Medical and Health Sciences University of Auckland Auckland New Zealand

2. Ophthalmology Greenlane Clinical Centre, Te Whatu Ora – Health New Zealand Auckland New Zealand

3. Radiology Auckland City Hospital, Te Whatu Ora – Health New Zealand Auckland New Zealand

4. Paediatrics Waitemata, Te Whatu Ora – Health New Zealand Auckland New Zealand

5. Paediatrics Counties Manukau, Te Whatu Ora – Health New Zealand Auckland New Zealand

6. Paediatric Neurology Starship Childrens Hospital, Te Whatu Ora – Health New Zealand Auckland New Zealand

7. Paediatric Neurosurgery Starship Childrens Hospital, Te Whatu Ora – Health New Zealand Auckland New Zealand

Abstract

AimHypovitaminosis A is a leading cause of preventable childhood blindness, especially in developing nations. Vitamin A is a fat‐soluble essential micronutrient that serves vital functions in the visual system and in regulating bone resorption. We report on a series of four children with mixed nutritional and compressive optic neuropathy and provide a review of the literature.MethodsA retrospective observational study of four males (ages 9–12), three with autism spectrum disorder who presented with loss of vision and multiple vitamin deficiencies including hypovitaminosis A.ResultsPatients presented with unexplained visual loss or a change in visual behaviour. All patients had severely restricted diet comprising of predominantly carbohydrates. Two of the four cases demonstrated optic nerve pallor at initial presentation with marked optic atrophy developing in all patients over time. Electrophysiology available in two patients demonstrated optic nerve dysfunction with preserved retinal function. Extensive investigations revealed profound deficiency in multiple vitamins including vitamin A (<0.1–0.2 μmol/L, normal = 0.9–1.7 μmol/L). Three patients also had low vitamin B12 (90–111 pmol/L, normal = 170–800 pmol/L) with normal folate. All four cases had radiological evidence of skull base thickening indicative of low vitamin A. Genetic testing did not find any relevant pathogenic variants.ConclusionsHypovitaminosis A is a crucial form of nutritional deprivation that results in significant visual loss with potential hyperostosis and optic nerve compression exacerbating nutritional optic neuropathy. Additional micronutrient deficiencies usually co‐exist and may contribute. Extra vigilance in vitamin replacement is required of clinicians with patients with autism who have restricted diets.

Publisher

Wiley

Reference48 articles.

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3. Genome‐wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy;Afshari NA;Nat. Commun.,2017

4. World Health Organization.International classification of diseases for mortality and morbidity statistics (11th revision).2018.

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