Eyelid Lesions in Lipoid Proteinosis or Urbach-Wiethe Disease: Case Report and Review of the Literature
Author:
Publisher
Informa UK Limited
Subject
Ophthalmology
Link
http://www.tandfonline.com/doi/pdf/10.3109/01676830.2011.579685
Reference8 articles.
1. Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)
2. Dry Eye Syndrome Associated With Urbach-Wiethe Disease
3. Bilateral lens subluxation in a case of lipoid proteinosis
4. Lipoid Proteinosis:
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1. Moniliform blepharosis in lipoid proteinosis: A rare case;Indian Journal of Ophthalmology - Case Reports;2023
2. Evaluation of choroidal thickness and ocular manifestations in lipoid proteinosis;International Ophthalmology;2022-07-17
3. Lipoid Proteinosis presenting as beaded papules of the eyelid: report of three cases;BMC Ophthalmology;2021-01-13
4. Biopsy of the Eyelid, the Lacrimal Sac, and the Temporal Artery;Lee's Ophthalmic Histopathology;2021
5. Lipoid Proteinosis: A Rare Disease In Pediatric Dentistry;Brazilian Dental Journal;2020-04
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