CACNA1F-related synaptic dysfunction: challenges diagnosing congenital stationary night blindness presenting without night blindness.
Journal
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie
ISSN: 1715-3360
Titre abrégé: Can J Ophthalmol
Pays: England
ID NLM: 0045312
Informations de publication
Date de publication:
27 Dec 2023
27 Dec 2023
Historique:
received:
31
10
2023
accepted:
26
11
2023
medline:
2
1
2024
pubmed:
2
1
2024
entrez:
30
12
2023
Statut:
aheadofprint
Résumé
Describe pediatric patients with CACNA1F-associated incomplete X-linked congenital stationary night blindness presenting without nyctalopia, and review the causes leading to diagnosis delay. Retrospective cohort. This was set in a single institution between 2004 and 2019. There were12 patients. The intervention or observation procedures used were clinical course, visual acuity, refractive error, images, electrophysiology, genetic testing, pedigree. The main outcome measures were cohort description and causes of diagnosis delay. For these 12 cases, the referring diagnosis was congenital nystagmus (7), reduced best-corrected visual acuity (BCVA, 4), and progressive myopia (1). Nyctalopia was not a presenting symptom and developed in 4 patients during follow-up. Seven patients presented with nystagmus. All patients developed early-onset myopia. Myopia progressed more rapidly before age 6 than after (average 1.14 D vs 0.25 D) (p = 0.0033). The average final BCVA was 20/50 (20/30-20/150). Vision at presentation was correlated with final visual acuity (r In children, CACNA1F-associated synaptic dysfunction does not usually present with night blindness. It should be suspected in male patients with early-onset myopia, especially with a history of nystagmus.
Identifiants
pubmed: 38159912
pii: S0008-4182(23)00382-4
doi: 10.1016/j.jcjo.2023.11.022
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2023 Canadian Ophthalmological Society. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Footnotes and Disclosure Funding/Support: Dr. Drack is supported by Ronald Keech Professorship. Dr. Dumitrescu is supported by Chakraborty Family Professor in Pediatric Genetic Retinal Diseases. Financial Disclosures: Alina Dumitrescu: Consultant for PureTech Health Inc. (Boston, MA ReVision Therapeutics Inc. (Ridgewood, NJ). Advisory board Janssen Pharmaceutica (Titusville, NJ). Arlene Drack: Research Grants Chakraborty Family Foundation, Fighting Blindness Canada, InVision2020, Spark Therapeutics, Regeneron. Advisory Board NOAH and ProQr. Wanda L Pfeifer: Employee of iScreen Vision Inc. Memphis TN. Monica Arhens—No financial disclosures. Jeaneen L Andorf—No financial disclosures.