Tfos dews ii pathophysiology report

AJ Bron, CS de Paiva, SK Chauhan, S Bonini… - The ocular …, 2017 - Elsevier
Abstract The TFOS DEWS II Pathophysiology Subcommittee reviewed the mechanisms
involved in the initiation and perpetuation of dry eye disease. Its central mechanism is …

[HTML][HTML] A systematic literature review of the disease burden in patients with recessive dystrophic epidermolysis bullosa

JY Tang, MP Marinkovich, E Lucas, E Gorell… - Orphanet journal of rare …, 2021 - Springer
Background/objective Recessive dystrophic epidermolysis bullosa (RDEB) is a genetic
collagen disorder characterized by skin fragility leading to blistering, wounds, and scarring …

Eye involvement and management in inherited epidermolysis bullosa

Y Bachir, A Daruich, C Marie, MP Robert… - Drugs, 2022 - Springer
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 …

Extended wear bandage contact lenses decrease pain and preserve vision in patients with epidermolysis bullosa: case series and review of literature

R Rashad, MC Weed, N Quinn… - Ocular Immunology and …, 2020 - Taylor & Francis
Purpose: To demonstrate the therapeutic benefit of extended wear bandage contact lens
(BCL) use in patients with epidermolysis bullosa (EB) suffering from recurrent, painful, and …

[HTML][HTML] Raising awareness among healthcare providers about epidermolysis bullosa and advancing toward a cure

A Tabor, JV Pergolizzi Jr, G Marti… - The Journal of …, 2017 - ncbi.nlm.nih.gov
Objective: Epidermolysis bullosa (EB) is an orphan disease that affects about half a million
people worldwide, but may not be familiar to all clinicians. The authors' goal was to present …

[HTML][HTML] A review of scoring systems for ocular involvement in chronic cutaneous bullous diseases

BWH Lee, JCK Tan, M Radjenovic, MT Coroneo… - Orphanet journal of rare …, 2018 - Springer
Background Epidermolysis bullosa (EB) and autoimmune blistering diseases (AIBD)
describe a group of rare chronic dermatoses characterized by cutaneous fragility and …

Pediatric ophthalmoplegia and ptosis in epidermolysis bullosa simplex associated with muscular dystrophy

W Al-Thawabieh, AW Lucky, B Wong… - Journal of Pediatric …, 2018 - journals.healio.com
Oculomotor dysfunction in epidermolysis bullosa simplex associated with muscular
dystrophy has been reported rarely in the ophthalmic literature. In a series of 6 patients with …

[PDF][PDF] TFOS DEWS II pathophysiology report

Y Ogawa, V Perez, Y Uchino, N Yokoi, D Zoukhri… - Ocular …, 2017 - app.aico.swiss
abstract The TFOS DEWS II Pathophysiology Subcommittee reviewed the mechanisms
involved in the initiation and perpetuation of dry eye disease. Its central mechanism is …

[PDF][PDF] DEWS II

A Bron - Ocular Surface, 2017 - tfosdewsreport.org
TFOS DEWS II - DE Pathophysiology_DE Page 1 Translated into German by Allergan DEWS II
Übersetzung Ursprünglich Bron A et al., TFOS DEWS II http://dx.doi.org/1 TFOS möchte die …

[PDF][PDF] Dysfonction des glandes de Meibomius de l'enfant

D Bremond-Gignac - cahiers-ophtalmologie.fr
Chez l'enfant les dysfonctions des glandes de Meibomius (DGM) sont souvent sous-éva-
luées et sous-diagnostiquées. Les chalazions récidivants représentent les premières …