A Diagnostic Challenge: Recurrent Uveitis Leading to the Diagnosis of Hyper-IgD Syndrome in a 28-Year-Old Patient

Recurrent uveitis, even in adult patients, should prompt the investigation of rare autoinflammatory syndromes. A timely genetic diagnosis and a multidisciplinary approach are crucial for initiating targeted biological treatments, which offer a superior visual and systemic prognosis compared to conventional therapies.

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Publication Details

Journal
Ocular Immunology and Inflammation
Published
2026-02-04
DOI
https://doi.org/10.1080/09273948.2026.2625998
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
Field-Weighted Citation Impact
0.00
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article

A Diagnostic Challenge: Recurrent Uveitis Leading to the Diagnosis of Hyper-IgD Syndrome in a 28-Year-Old Patient

E. Rico Santos, María José Esteban Giner, Marta Mifsut Aleixandre, Teresa De Paz Aguilera et al.
Ocular Immunology and Inflammation
Ocular Diseases and Behçet’s Syndrome
article

A Diagnostic Challenge: Recurrent Uveitis Leading to the Diagnosis of Hyper-IgD Syndrome in a 28-Year-Old Patient

E. Rico Santos, María José Esteban Giner, Marta Mifsut Aleixandre, Teresa De Paz Aguilera, Jorge Salvo Jiménez
article en

Abstract

Recurrent uveitis, even in adult patients, should prompt the investigation of rare autoinflammatory syndromes. A timely genetic diagnosis and a multidisciplinary approach are crucial for initiating targeted biological treatments, which offer a superior visual and systemic prognosis compared to conventional therapies.

Ocular Immunology and InflammationVol. 34(3)
Hospital Virgen de los Lirios (ES)
Good health and well-being
Openalex Percentile: Top 67%
Ocular Diseases and Behçet’s Syndrome
DOISourceOpenAlex
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