Foveal hypoplasia in parents of patients with albinism

• Published in: Ophthalmic genetics Vol. 43; no. 6; pp. 817 - 823
• Main Authors: Lejoyeux, R, Alonso, A-S, Lafolie, J, Michaud, V, Lasseaux, E, Vasseur, V, Derrien, S, Robert, M P, Le Mer, Y, Tadayoni, R, Arveiler, B, Mauget-Faÿsse, M
• Format: Journal Article
• Language: English
• Published: England 01.12.2022
• Subjects: Albinism - genetics; Albinism, Ocular - diagnosis; Albinism, Ocular - genetics; Albinism, Oculocutaneous - diagnosis; Albinism, Oculocutaneous - genetics; Fovea Centralis - abnormalities; Humans; Retina; Tomography, Optical Coherence - methods; Vision Disorders - diagnosis; Foveal hypoplasia; fovea plana; foveal avascular zone; albinism
• ISSN: 1381-6810; 1744-5094
• DOI: 10.1080/13816810.2022.2121841

Albinism is a group of genetic disorders characterized by general skin and retinal hypopigmentation. It is in most cases an autosomal recessive condition. Foveal hypoplasia (FH) is one of the main criteria for the diagnosis of albinism. The aim of this study was to analyze the macular profile of the parents of patients with albinism. This study included a case series of 27 patients with albinism seen in Rothschild Foundation between April 2017 and February 2020. Spectral-domain optical coherence tomography (SD-OCT) and OCT angiography (OCT-A) were performed in every patient when possible and in every available parents. FH was graded according to Thomas' classification based on OCT. Next generation sequencing-based gene panel testing was performed in parents and children when a FH was detected on OCT in a parent. Twenty-seven patients with albinism were examined. Nine parents had FH based on the OCT B-scan (33%). In parents without FH based on the SD-OCT B-scan (67%), OCT-A showed a reduced avascular zone in the deep vascular plexus in 4 parents. Six parents carried variants that could explain their phenotype, including TYR R402Q hypomorphic alleles. This study showed the presence of FH in parents of patients with albinism, and aimed to genetically explain this phenotype.