Results 21 to 30 of about 2,133 (164)

A case of reversible toxic optic neuropathy from tacrolimus (FK506)

American Journal of Ophthalmology Case Reports, 2020
Purpose: To report a rare case of reversible vision loss from tacrolimus-associated toxic optic neuropathy. Observations: A 30-year-old man with cystic fibrosis requiring bilateral lung transplantation developed painless, bilateral, gradual onset central
Kimberly K. Gokoffski, MD, PhD, Vivek R. Patel, MD   +1 more
doaj   +1 more source

Alice in Wonderland and Ekbom Syndromes in a Bipolar I Manic Episode: A Case Report With Neuroimaging Findings. [PDF]

Case Rep Psychiatry
With recent advances in anatomical and functional brain mapping, Alice in Wonderland syndrome (AIWS), a perceptual distortion disorder, has received increased attention. We report the case of a 67‐year‐old man with bipolar I disorder (manic episode), AIWS, and delusional parasitosis (Ekbom syndrome). The patient exhibited diverse perceptual distortions
Hori Y, Yanagaki S, Nibuya M, Nakagawa S, Suzuki E.   +4 more
europepmc   +2 more sources

Dyschromatopsia in the Split-Dalmatia County [PDF]

, 2018
CILJ ISTRAŽIVANJA: Ispitati razinu zastupljenosti najčešćih klornih poremećaja: protanomalije u odnosu na deuteranomaliju na području Splitsko-dalmatinske županije i obratiti pozornost šire javnosti na važnost pravovremene detekcije poremećaja kolornog ...
Barać, Iva
core   +3 more sources

Prevalence and lack of awareness of dyschromatopsia among students of four university courses [PDF]

Revista Brasileira de Oftalmologia
Objective: To identify the prevalence of colour dyschromatopsia in students of engineering, medicine, dentistry, and pedagogy courses at a community college in a city in the Midwest of Santa Catarina, Brazil.
Arthur Gabriel Duran, Luísa Trucolo, Caio Antônio Nhoatto, Gabriel Gardini Fagundes Marafon, Fabricio Salazar Fiorio Marques, Luiz Henrique Paza da Costa, Ricardo Alexandre Stock, Antuani Rafael Baptistella, Elcio Luiz Bonamigo   +8 more
doaj   +2 more sources

Visão das cores em escolares: avaliação de um novo teste Color vision in school-age children: evalution a new test

Jornal de Pediatria, 2001
OBJETIVO: comparar os resultados de um teste de visão de cores padrão (teste de Ishihara) com um teste criado pelos autores (teste do giz de cera) na detecção da discromatopsia congênita.
Guilherme M. Martins, Marcela F. Bordaberry, Zélia M.S Corrêa, Michel B. Mânica, Juliano C. Costa, Nelson Telichevesky, Ítalo M. Marcon   +6 more
doaj   +1 more source

Leber’s hereditary optic neuropathy - case report

Journal of Health Sciences, 2012
Leber’s hereditary optic neuropathy is a neuro-ophthalmological entity characterized by acute or subacute bilateral, not simultaneous visual loss with centro cekal scotoma and occasional further visual improvement.
Mirjana A. Janicijevic Petrovic, Tatjana Sarenac Vulovic, Nenad Petrovic, Suncica Sreckovic, Svetlana Paunovic, Katarina Janicijevic, Dejan Vulovic, Dragan Vujic   +7 more
doaj   +3 more sources

ASSESSMENT OF COLOR VISION FOR DIAGNOSIS AND DYNAMIC MONITORING OF MULTIPLE SCLEROSIS

Alʹmanah Kliničeskoj Mediciny, 2016
Background: Multiple sclerosis is regarded as the most frequent cause of neurological disability. Visual disturbances are common and may be due to pathology of retina, optic nerve and cerebral conduction tracts (optic tract).
N. V. Kuchina, T. I. Yakushina, S. V. Kotov, D. G. Lapitan, O. M. Andryukhina, A. A. Ryabtseva   +5 more
doaj   +1 more source

Leber's hereditary optic neuropathy with complete visual recovery - the first report [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2021
Introduction. Leber’s hereditary optic neuropathy (LHON) typically affects young adults, with a higher prevalence in men, but can ultimately occur at any age, as well as in women. LHON is caused by point mutations in the mitochondrial DNA.
Kalezić Tanja, Maraš Željko, Karamarković Nemanja, Jeremić Miroslav, Bila Mladen   +4 more
doaj   +1 more source

Neuro-Ophthalmologic Variability in Presentation of Genetically Confirmed Wolfram Syndrome: A Case Series and Review

Brain Sciences, 2023
Wolfram syndrome is a neurodegenerative disorder caused by pathogenic variants in the genes WFS1 or CISD2. Clinically, the classic phenotype is composed of optic atrophy, diabetes mellitus type 1, diabetes insipidus, and deafness.
Ruben Jauregui, Nicolas J. Abreu, Shani Golan, Joseph F. Panarelli, Meenakshi Sigireddi, Gopi K. Nayak, Doria M. Gold, Janet C. Rucker, Steven L. Galetta, Scott N. Grossman   +9 more
doaj   +1 more source

Sirtuin 3 mutation- induced mitochondrial dysfunction and optic neuropathy: a case report

BMC Ophthalmology, 2023
Background Mitochondrial optic neuropathy is characterized by painless, progressive, symmetrical central vision loss, and dyschromatopsia owing to mitochondrial dysfunction.
Bo Young Chun, Jung Moon Choi, Su-Kyeong Hwang, Soolienah Rhiu   +3 more
doaj   +1 more source