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Objective: Investigating the clinical features and etiological diagnosis of early isolated ocular motor nerve palsy to deepen understanding of the condition.
Methods: We retrospectively enrolled 68 patients with isolated ocular motor nerve palsy admitted our hospital between 2017 and 2024. A retrospective analysis was conducted to assess their clinical and imaging characteristics. Based on current diagnostic criteria, patients were categorized into one of the following groups: diabetic ophthalmoplegia (DO), microvascular ocular motor nerve palsies (MVP), or Tolosa-Hunt syndrome (THS). Patients were divided into two groups based on the presence of diabetes, and the clinical and imaging differences between the two groups were compared.
Results: Of the 68 patients, 40 were male, with an average age of 61 years. There were 43 patients with diabetes, and 40 had a history of hypertension. The number of patients with isolated 3rd, 4th, and 6th nerve palsy was 42, 15, and 11, respectively. Sixty patients experienced headache or orbital pain. 46 patients met the criteria for MVP. Among them, 31 patients had DO, and 15 non-diabetic patients also met the criteria for MVP. Of the 46 patients, 22 showed abnormalities on contrast-enhanced MRI. 19 patients were diagnosed with THS. In the diabetic and non-diabetic groups, 11 and 9 patients, respectively, were diagnosed with THS. The number of patients receiving steroid treatment in the diabetic and non-diabetic groups was 38 and 23, respectively, with pain relief rates within 3 days of 70 and 56%, > 0.05.
Conclusion: Currently, the boundaries between DO, MVP, diabetes combined with THS, and benign THS remain unclear. There is a need for clinical research involving specialists in neurology, ophthalmology, and otolaryngology to establish standardized definitions, classifications, and diagnostic criteria.
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http://dx.doi.org/10.3389/fneur.2025.1592993 | DOI Listing |
Strabismus
September 2025
Department of Ophthalmology, Barcelona Hospital, Barcelona University, Barcelona, Spain.
: We report a case of an unusual association between Duane retraction syndrome and Marcus Gunn jaw-winking syndrome in the eye of a patient without other anomalies.: Clinical case. A four-year-old boy presented mild blepharoptosis of the left upper eyelid.
View Article and Find Full Text PDFJ Head Trauma Rehabil
September 2025
Author Affiliations: Hearing Center of Excellence, Joint Base San Antonio-Lackland Air Force Base, Texas (Dr Lambert); Advanced Exposures, Diagnostics, Interventions, and Biosecurity (AEGIS) Program, Joint Base San Antonio-Lackland Air Force Base, Texas (Dr Hoppes); Department of Orthopaedic Surgery
Objective: This study examined false-positive rates and associated factors on the Vestibular/Ocular Motor Screening (VOMS) in healthy US Army Special Operations Command (USASOC) personnel using the symptom provocation cutoff of ≥1 for any VOMS item as recommended in the Military Acute Concussion Evaluation 2 (MACE 2).
Setting: Military site.
Participants: Active-duty USASOC personnel aged 18 to 40 years with 20/20 vision, no duty limitations, and no recent concussion.
Cerebellum
September 2025
Department of Neurology, The Johns Hopkins School of Medicine, Baltimore, MD, USA.
Spinocerebellar ataxia type 27B (SCA27B), caused by GAA repeat expansions in FGF14, is an increasingly recognized form of late-onset cerebellar ataxia. However, early diagnosis remains challenging due to mild or absent cerebellar motor signs and often normal brain magnetic resonance imaging (MRI). Oculovestibular abnormalities, although prevalent, are frequently overlooked and not captured by standard clinical scales such as the Scale for the Assessment and Rating of Ataxia (SARA).
View Article and Find Full Text PDFParasitol Res
September 2025
Medical Parasitology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.
Human toxocariasis presents in several forms, including visceral larva migrans, ocular larva migrans, covert toxocariasis, and neurotoxocariasis. Although several studies suggest a potential link between toxocariasis and epilepsy, this link is still debated. Additional mechanistic and experimental studies in animal models are essential for a better understanding of this association.
View Article and Find Full Text PDFEur J Paediatr Neurol
August 2025
University Hospital for Infectious Diseases "Dr. Fran Mihaljević", Mirogojska 8, 10000, Zagreb, Croatia; University of Zagreb, School of Medicine, Šalata 3, 10000, Zagreb, Croatia.
Background: Acute disseminated encephalomyelitis (ADEM) is a rare disease characterized by encephalopathy, polyfocal symptoms and demyelination. Although its prognosis is generally favorable, there is growing evidence that subtle neuropsychological and motoric sequelae may persist years after the initial episode.
Aim: To assess the relationship between clinical, laboratory and radiological characteristics of the acute monophasic ADEM episode in children, and its immediate outcome, and long(er) term disability/functional status.