Results 21 to 30 of about 35,344 (269)

Cogan’s anterior internuclear ophthalmoplegia in young Ethiopian: A case report and review of literature

open access: yesAlexandria Journal of Medicine, 2014
Introduction: Lesions in medial longitudinal fasciculus (MLF) produce internuclear ophthalmoplegia (INO) with characteristic horizontal gaze abnormality.
Yeshigeta Gelaw
doaj   +1 more source

Clinical efficacy of the partial rectus muscle transportation procedure for paralytic strabismus [PDF]

open access: yesInternational Journal of Ophthalmology, 2020
AIM: To analyze the clinical efficacy of the partial rectus muscle transportation (PRT) procedure for paralytic strabismus due to single rectus muscle palsy.
Yan-Qiong Tu   +3 more
doaj   +1 more source

血管病相关性眼肌麻痹病因的研究进展 Study Progress of Etiology of Ophthalmoplegia Associated with Vascular Disease

open access: yesZhongguo cuzhong zazhi, 2018
眼肌麻痹是神经内科、眼科、神经眼科的常见体征。根据病变部位,血管病相关的眼肌 麻痹可分为核上型、核型、核间型、周围神经型,不同型别的眼肌麻痹有不同的病因。核上型、核型 及核间型眼肌麻痹多见于卒中,其中核型眼肌麻痹以动眼神经核受累最常见。周围神经型眼肌麻痹 病因众多,如糖尿病性眼肌麻痹、动脉瘤、颈内动脉海绵窦瘘等。糖尿病性眼肌麻痹多累及动眼神经, 瞳孔受累较轻,一般数周后开始恢复;动脉瘤和颈内动脉海绵窦瘘所致眼肌麻痹需行数字减影血管 造影(digital subraction angiography ...
李然,景筠
doaj   +1 more source

Neurotoxin envenomation mimicking brain death in a child: A case report and review of literature

open access: yesIndian Journal of Anaesthesia, 2014
The spectrum of presentation of a victim of neurotoxic snake bite can range from mild ptosis to complete paralysis and ophthalmoplegia. We report a case of snake bite in a 10-year-old child who was comatosed with bilateral fixed dilated pupils and absent
Madhu Dayal   +3 more
doaj   +1 more source

Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases

open access: yesThe Turkish Journal of Pediatrics, 2022
Background. Recurrent painful ophthalmologic neuropathy (RPON), formerly known as ophthalmoplegic migraine, is characterized by repeated attacks of one or more ocular cranial nerve palsies with an ipsilateral headache.
Çağatay Günay   +4 more
doaj   +1 more source

Carotid cavernous fistula: A rare but treatable cause of ophthalmoplegia - A case report

open access: yesBrain Circulation, 2023
Carotid cavernous fistulas (CCFs) are a rare but debilitating entity that may present with orbital or cerebral venous hypertension. CCFs may pose diagnostic and management pitfalls for clinicians as they can initially be misdiagnosed as primary orbital ...
Neeharika Krothapalli   +5 more
doaj   +1 more source

Congenital fibrosis of the extraocular muscles

open access: yesOman Journal of Ophthalmology, 2010
Background : Congenital fibrosis of the extraocular muscles (CFEOM) describes a group of rare congenital eye movement disorders that result from the dysfunction of all or part of the oculomotor (CN 3) and the trochlear (CN 4) nerves, and/or the muscles ...
Pascale Cooymans   +3 more
doaj   +1 more source

Assessment of the prevalence and risk factors of ophthalmoplegia among diabetic patients in a large national diabetes registry cohort

open access: yesBMC Ophthalmology, 2016
BackgroundThere are limited data on the epidemiology and risk factors of ophthalmoplegia among diabetic patients. This study aims to determine the prevalence and important risk factors related to ophthalmoplegia among diabetic patients.MethodsThis is an ...
Eman Alkahtani   +5 more
semanticscholar   +1 more source

Síndrome do ápice orbitário causada por herpes zóster oftálmico: relato de caso e revisão da literatura Herpes zoster ophthalmicus and orbital apex syndrome: case report and literature review

open access: yesRevista Brasileira de Oftalmologia, 2009
OHerpes Zoster Oftálmico (HZO) decorre da infecção pelo vírus da varicela-zoster que permanece latente no gânglio de Gasser até que seja reativado e comprometa a divisão oftálmica do nervo trigêmeo.
Kenzo Hokazono   +3 more
doaj   +1 more source

MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form

open access: yesMolecular Genetics & Genomic Medicine, 2020
Background Hereditary myosin myopathies are a group of rare muscle disorders, caused by mutations in genes encoding for skeletal myosin heavy chains (MyHCs). MyHCIIa is encoded by MYH2 and is expressed in fast type 2A and 2B muscle fibers. MYH2 mutations
Roberta Telese   +12 more
doaj   +1 more source

Home - About - Disclaimer - Privacy