Publications by authors named "S Akkus"

Objective: To assess the demographic, clinical, and outcome data in patients with NMOSD across a single-center adult cohort and find out associations, if any, with the disease burden.

Background: Neuromyelitis Optica spectrum disorder is an autoimmune condition with unpredictable course and relapses. The clinical and economic burden of NMOSD has been studied less.

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Background: This descriptive analysis examines the victims of the February 6, 2023, earthquakes in Kahramanmaraş and Elbistan, Türkiye. It aims to detail the injury profiles related to neuro-musculoskeletal trauma, assess the rehabilitation needs of patients, and propose a comprehensive rehabilitation approach.

Methods: The study included patients injured in the Kahramanmaraş-centered earthquake on February 6, 2023, who were transported to our hospital based on their rehabilitation needs.

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Parry-Romberg Syndrome (PRS) is a rare neurocutaneous disorder characterized by gradual facial hemiatrophy. We present a case study of a 64-year-old woman with late-onset PRS and linear scleroderma. The patient exhibited atypical PRS symptoms including leg numbness, hyper-reflexia, trigeminal neuralgia, and severe headaches.

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Introduction: Paraneoplastic neurologic syndromes (PNS) and autoimmune encephalitis (AIE) are immune-mediated disorders. PNS is linked to cancer, while AIE may not Their clinical manifestations and imaging patterns need further elucidation.

Objective/aims: To investigate the clinical profiles, antibody associations, neuroimaging patterns, treatments, and outcomes of PNS and AIE.

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Article Synopsis
  • The study aimed to identify and describe uncommon manifestations in patients with atypical parkinsonian syndromes by analyzing medical records over more than a decade.
  • A total of 46 patients with atypical symptoms were analyzed, with diagnoses including multiple system atrophy, dementia with Lewy bodies, frontotemporal dementia, corticobasal syndrome, and progressive supranuclear palsy.
  • Results indicated similar prevalence of atypical findings across the different syndromes, highlighting features like myoclonus, double vision, and abnormal MRI signs, suggesting some cases may have genetic implications.
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