Eye Involvement and Management in Inherited Epidermolysis Bullosa

被引：3

作者：

Bachir, Yasmine ^{[1
]}

Daruich, Alejandra ^{[1
,2
]}

Marie, Couanon ^{[1
]}

Robert, Matthieu P. ^{[1
]}

Bremond-Gignac, Dominique ^{[1
,2
]}

机构：

[1] Paris Cite Univ, Necker Enfants Malad Univ Hosp, AP HP, Ophthalmol Dept, 149 Rue Sevres, F-75015 Paris, France

[2] Sorbonne Paris Cite Univ, Physiopathol Ocular Dis Clin Dev, Team 17, UMRS1138,INSERM,Ctr Rech Cordeliers, Paris, France

来源：

DRUGS | 2022年 / 82卷 / 12期

关键词：

KINDLER SYNDROME; COMPLICATIONS; DIAGNOSIS; KERATOPROSTHESIS; TRANSPLANTATION; MANIFESTATIONS; CLASSIFICATION; FREQUENCY; GENOTYPE; FEATURES;

D O I：

10.1007/s40265-022-01770-8

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Inherited epidermolysis bullosa (EB) is a group of genetic rare diseases associated with skin fragility, which leads to the formation of blisters, erosions, and scars on the skin and mucous membranes. Epidermolysis bullosa includes four main types and some several clinical subtypes including EB simplex, junctional EB, dystrophic EB, and Kindler's EB. Ocular involvement ranged from 51 to 68% in EB and can cause irreversible damages if not properly managed. Corneal erosions are the most common finding among series, including our cohort. We review here clinical and pathological features of ocular involvement in EB and the main keys for management, with a focus on recent innovative therapies.

引用

页码：1277 / 1285

页数：9

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