Results 51 to 60 of about 18,947 (252)

Optic disc drusen in children: a diagnostic challenge [PDF]

open access: yesRevista Brasileira de Oftalmologia, 2020
In children, optic disc drusen (ODD) are often mistaken for papilledema, this being the prin-cipal differential diagnosis. This report describes the case of an 11-year old patient with ODD, in which the condition was initially diagnosed as papilledema ...
Priscilla Fernandes Nogueira   +4 more
doaj   +2 more sources

Crowded Disc in a High Hyperopic Patient Misdiagnosed as Papilledema [PDF]

open access: yes, 2019
A 16 year old female was referred to neurological clinic with diagnosis of papilledema for neurological evaluation. After consultation with us we became suspicious of pseudopapilledema according to refraction and biometric characteristics of the eye and ...
Attarian, Behnoosh   +3 more
core   +2 more sources

Artificial Intelligence to Detect Papilledema from Ocular Fundus Photographs. [PDF]

open access: yes, 2020
BACKGROUND: Nonophthalmologist physicians do not confidently perform direct ophthalmoscopy. The use of artificial intelligence to detect papilledema and other optic-disk abnormalities from fundus photographs has not been well studied. METHODS: We trained,
Aghsaei Fard, Masoud   +36 more
core   +2 more sources

Diagnosis of papilledema and pseudopapilledema using optical coherence tomography [PDF]

open access: yes, 2022
Background: Papilledema is a common clinical problem where the ophthalmologist plays an important role in its diagnosis. Optical coherence tomography (OCT) provides high resolution images of the retina and the retinal nerve fiber layer (RNFL).Objective ...
Al-Nashar, Haitham Younis   +3 more
core   +1 more source

Fluvoxamine-induced intracranial hypertension in a 10-year-old boy

open access: yesIndian Journal of Ophthalmology, 2018
Drug-induced intracranial hypertension is a well-established entity. We report a rare case of intracranial hypertension with papilledema in a 10-year-old boy following use of fluvoxamine, a selective serotonin reuptake inhibitor.
Hemalini Samant, Preetam Samant
doaj   +1 more source

Transverse venous sinus stenting for idiopathic intracranial hypertension: Safety and feasibility [PDF]

open access: yes, 2018
Purpose Transverse sinus stenosis is commonly seen in patients with idiopathic intracranial hypertension. It is not clear whether it is the cause or the result of idiopathic intracranial hypertension. Stenting for idiopathic intracranial hypertension has
Koovor, Jerry ME   +3 more
core   +1 more source

Postnatal Progressive Craniosynostosis: An Unusual Case Presentation Leading to Cascade Diagnosis for Multiple Generations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT NM_000141.5: FGFR2 c.1032G>A is a pathogenic variant that causes Crouzon syndrome through activation of a new donor splice site. This clinical report highlights the intrafamilial variability that can exist with this specific variant. The proband is a 4‐year‐old boy who initially presented with concern for seizures.
Jessica T. Ogawa   +3 more
wiley   +1 more source

The Interconnected World of Dermatology and Ophthalmology

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Medicine is a dynamic field that constantly discovers new links between different specialties. Dermatology and Ophthalmology are two related branches of medicine, having many similarities and interactions. The skin and the eyes both encounter various environmental challenges, such as ultraviolet radiation, allergens, infections, and trauma ...
Gyanesh Rathore   +4 more
wiley   +1 more source

The diagnostic challenge of evaluating papilledema in the pediatric patient

open access: yesTaiwan Journal of Ophthalmology, 2017
Pseudopapilledema is a fairly common finding in ophthalmic practice, and in many cases, the diagnosis is straightforward. However, an accurate diagnosis can challenge the most seasoned clinicians, and missing true papilledema can result in life ...
Brandon McCafferty   +2 more
doaj   +1 more source

Neonatal-onset multisystem inflammatory disease responsive to interleukin-1 beta inhibition [PDF]

open access: yes, 2006
BACKGROUND:Neonatal-onset multisystem inflammatory disease is characterized by fever, urticarial rash, aseptic meningitis, deforming arthropathy, hearing loss, and mental retardation.
Adams, BS   +39 more
core  

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