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
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.

Auteurs

Alina V Dumitrescu (AV)

Department of Ophthalmology, University of Iowa, Iowa City, Iowa. Electronic address: alina-dumitrescu@uiowa.edu.

Wanda L Pfeifer (WL)

Department of Ophthalmology, University of Iowa, Iowa City, Iowa.

Monica Arhens (M)

Department of Biostatistics, University of Iowa, Iowa City, Iowa.

Jeaneen L Andorf (JL)

Institute for Vision Research, University of Iowa, Iowa City, Iowa.

Arlene V Drack (AV)

Department of Ophthalmology, University of Iowa, Iowa City, Iowa; Department of Biostatistics, University of Iowa, Iowa City, Iowa.

Classifications MeSH