Torpedo maculopathy in a patient with DeSanto-Shinawi syndrome

IntroductionTorpedo maculopathy (TM) is a rare, typically benign and congenital anomaly of the retinal pigment epithelium (RPE) characterized by a torpedo-shaped lesion in the macula. DeSanto-Shinawi syndrome (DESS) is an equally rare genetic disorder caused by mutations in the WAC gene, presenting with intellectual disability, dysmorphic features, and growth retardation.Case descriptionThis report illustrates the case of monolateral TM in a patient with DESS. The genetic and phenotypic characteristic were described and correlated with retinal features, assessed by means of retinography, spectral domain OCT (SD-OCT) and fluorescein angiography (FA).ConclusionThis case report discusses the unusual co-occurrence of TM in a patient diagnosed with DESS, contributing to the sparse literature on this association and expanding the phenotypic spectrum of both conditions.

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Publication Details

Journal
European Journal of Ophthalmology
Published
2025-02-12
DOI
https://doi.org/10.1177/11206721251313840
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Torpedo maculopathy in a patient with DeSanto-Shinawi syndrome

Gaetano Zinzanella, Paola Valente, Giancarlo Iarossi, Sergio Petroni et al.
European Journal of Ophthalmology
Retinal Development and Disorders
article

Torpedo maculopathy in a patient with DeSanto-Shinawi syndrome

Gaetano Zinzanella, Paola Valente, Giancarlo Iarossi, Sergio Petroni, Matteo Federici, Luca Buzzonetti, Carlo Maria De Sanctis, G. Catena
article en

Abstract

IntroductionTorpedo maculopathy (TM) is a rare, typically benign and congenital anomaly of the retinal pigment epithelium (RPE) characterized by a torpedo-shaped lesion in the macula. DeSanto-Shinawi syndrome (DESS) is an equally rare genetic disorder caused by mutations in the WAC gene, presenting with intellectual disability, dysmorphic features, and growth retardation.Case descriptionThis report illustrates the case of monolateral TM in a patient with DESS. The genetic and phenotypic characteristic were described and correlated with retinal features, assessed by means of retinography, spectral domain OCT (SD-OCT) and fluorescein angiography (FA).ConclusionThis case report discusses the unusual co-occurrence of TM in a patient diagnosed with DESS, contributing to the sparse literature on this association and expanding the phenotypic spectrum of both conditions.

European Journal of OphthalmologyVol. 35(3)
Bambino Gesù Children's Hospital (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT)
Ministero della Salute
Good health and well-being
Openalex Percentile: Top 98%
Retinal Development and Disorders
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