Results 61 to 70 of about 1,359,849 (169)
ABSTRACT Immune homeostasis is indispensable for preserving organismal integrity, orchestrated through complex molecular networks encompassing immune cell dynamics, microbial cues, and epigenetic regulation. Among these, the gut microbiota‐non‐coding RNA (ncRNA) axis has recently garnered substantial attention as a multifaceted modulator of host ...
Bonan Chen +12 more
wiley +1 more source
The Role of Viral and Bacterial Infections in the Etiology of Behçet's Disease
Bacterial and viral pathogens may play a key role in Behçet's disease (BD) pathogenesis by triggering autoimmunity, molecular mimicry, or microbiome disruption. These infectious agents could initiate inflammatory pathways, contributing to BD's diverse clinical manifestations.
Mohsen Moghoofei +4 more
wiley +1 more source
Vogt-Koyanagi-Harada Syndrome. An unusual case with lacquer crack-like retinal findings
We report the case of a 35-year-old female patient with bilateral and recurrent panuveitis. Diagnosed with Vogt-Koyanagi-Harada syndrome, the patient was treated with corticosteroids, achieving rapid improvement of functional and morphological findings ...
Kocaoglu, G. +2 more
core +1 more source
Q fever: a new ocular manifestation
P Udaondo1,3, S Garcia-Delpech1,2, D Salom1,2, M Garcia-Pous1, M Diaz-Llopis1,21Department of Ophthalmology, Nuevo Hospital Universitario y Politecnico La Fe, Valencia, Spain; 2Faculty of Medicine, Universitat de València, Valencia, Spain ...
Udaondo P +4 more
doaj
Introduction We report a case of unilateral presumed nonarteritic anterior ischemic optic neuropathy (NAION) associated with acute posterior multifocal placoid pigment epitheliopathy (APMPPE). Case Presentation A 59‐year‐old female presented with blurred left vision for 9 days. At the initial examination, her best‐corrected visual acuities (BCVAs) were
Marie Ikeda +3 more
wiley +1 more source
Síndrome de Vogt-Koyanagi-Harada. Revisión a propósito de un caso [PDF]
Se realiza una revisión bibliográfica sobre el síndrome de Vogt-Koyanagi-Harada (VKH) a propósito de un caso clínico de un hombre de 37 años, comparando las características presentadas por el paciente con la bibliografía, para poder establecer una ...
García García-Arévalo, Miguel
core
A rare pediatric case of probable Vogt–Koyanagi–Harada syndrome
We report a rare case of probable Vogt–Koyanagi–Harada (VKH) syndrome in a 10-year-old child who presented with visual acuity of only perception of light present in both eyes.
Malarvizhi Raman +4 more
doaj +1 more source
Vogt–Koyanagi–Harada (VKH) syndrome: A new perspective for healthcare professionals
Vogt–Koyanagi–Harada syndrome (VKH syndrome) is a rare granulomatous inflammatory disease that affects the melanin pigment producing melanocytes and mainly affects the pigmented structures such as eyes, ear, skin, meninges, and hair. VKT is an autoimmune
Yojana B Patil +6 more
doaj +1 more source
Choroidal effusion is characterised by fluid accumulation in the suprachoroidal space and can be either idiopathic or associated with trauma, infection, inflammation or intraocular surgery. On rare occasions, this can cause a secondary angle‐closure glaucoma that does not involve a pupil block mechanism.
Umme Kalsoom Alam +5 more
wiley +1 more source
Vitiligo révélant une maladie de Vogt-Koyanagi-Harada
Le vitiligo est une dermatose chronique auto-immune, souvent associé ou fait découvrir d'autres pathologies auto-immunes. Son association à une atteinte ophtalmologique à type de pan uvéite et /ou une atteinte neurologique à type de méningite et/ou de l ...
Mohamed El Amraoui +5 more
doaj +1 more source

