Aland Island Eye Disease with Retinoschisis in the Clinical Spectrum of <i>CACNA1F</i>-Associated Retinopathy—A Case Report

Aland Island Eye Disease with Retinoschisis in the Clinical Spectrum of <i>CACNA1F</i>-Associated Retinopathy—A Case Report

Aland island eye disease (AIED), an incomplete form of X-linked congenital stationary night blindness (CSNB2A), and X-linked cone-rod dystrophy type 3 (CORDX3) display many overlapping clinical findings. They result from mutations in the <i>CACNA1F</i> gene encoding the α<sub>1F<...

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Bibliographic Details
Main Authors: Dorota Wyględowska-Promieńska, Marta Świerczyńska, Dorota Śpiewak, Dorota Pojda-Wilczek, Agnieszka Tronina, Mariola Dorecka, Adrian Smędowski
Format: Article
Language:English
Published: MDPI AG 2024-03-01
Series:International Journal of Molecular Sciences
Subjects:
Aland island eye disease
AIED
CACNA1F
Cav1.4
retinoschisis
Online Access:https://www.mdpi.com/1422-0067/25/5/2928

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