Journal Article

Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights

Bacci, Giacomo M., Caputo, Roberto, Fortunato, Pina, Tiberi, Lucia, Durand, Marine, Artuso, Rosangela, Sodi, Andrea, Paques, Michel, Stabile, Monica, Virgili, Gianni, Landini, Samuela, Peron, Angela, Pagliazzi, Angelica, Marziali, Elisa, Bargiacchi, Sara, Palazzo, Viviana, Vergani, Debora, Rocca, Camilla, Pacini, Bianca

2024

Overview

Aim of the present study is to evaluate the relationship between genetic and phenotypic data in a series of patients affected by grade I and II of foveal hypoplasia with stable fixation and good visual acuity using multimodal imaging techniques. All patients underwent complete clinical and instrumental assessment including structural Optical Coherence Tomography (OCT), OCT Angiography and Adaptive Optics (AO) imaging. Central macular thickness (CMT), inner nuclear layer (INL), vessel density in superficial capillary plexus were the main variables evaluated with OCT technology. Cone density, cone spacing, cone regularity, cone dispersion and angular density were the parameters evaluated with AO. Genetic evaluation and trio exome sequencing were performed in all affected individuals. Eight patients (3 males and 5 females) with a mean age of 12.62 years (range 8–18) were enrolled. The mean best corrected visual acuity (BCVA) was 0.18 ± 0.13 logMAR, mean CMT was 291.9 ± 16.6 µm and INL was 26.2 ± 4.6 µm. The absence of a foveal avascular zone (FAZ) was documented by examination of OCT-A in seven patients in the superficial capillary plexus. However, there was a partial FAZ in the deep plexus in patients P5 and P8. Of note, all the patients presented with major retinal vessels clearly crossing the foveal center. All individuals exhibited a grade I or II of foveal hypoplasia. In 5 patients molecular analyses showed an extremely mild form of albinism caused by compound heterozygosity of a TYR pathogenic variant and the hypomorphic p.[Ser192Tyr;Arg402Gln] haplotype. One patient had Waardenburg syndrome type 2A caused by a de novo variant in MITF. Two patients had inconclusive molecular analyses. All the patients displayed abnormalities on OCT-A. Photoreceptor count did not differ from normal subjects according to the current literature, but qualitative analysis of AO imaging showed distinctive features likely related to an abnormal pigment distribution in this subset of individuals. In patients with foveal hypoplasia, genetic and multimodal imaging data, including AO findings, can help understand the physiopathology of the foveal hypoplasia phenotype. This study confirms that cone density and visual function can both be preserved despite the absence of a pit.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 631/208/1516 / 692/420/2489/144 / 692/700/1720/3187 / Acuity / Adaptive optics / Adolescent / Albinism / Albinism - genetics / Angiography / Blood vessels / Child / Cone mosaic / Female / Fluorescein Angiography - methods / Fovea Centralis - abnormalities / Fovea Centralis - diagnostic imaging / Fovea Centralis - pathology / Foveal hypoplasia / Genetic analysis / Haplotypes / Heterozygosity / Humanities and Social Sciences / Humans / Hypoplasia / Male / multidisciplinary / Multimodal Imaging - methods / OCT / OCT-A / Optics / Patients / Pediatrics / Phenotype / Phenotypes / Phenotyping / Qualitative analysis / Science / Science (multidisciplinary) / Tomography, Optical Coherence - methods / TYR / Visual Acuity / Visual perception / Whole genome sequencing