Neural Networks and Rules-based Systems used to Find Rational and Scientific Correlations between being Here and Now with Afterlife Conditions
Neural Networks and Rules-based Systems used to Find Rational and
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We report a rare case of Wilson’s Disease with neurologic features in a 31-year-old man. This disease consists of a disturbance of copper metabolism secondary to a mutation in the gene responsible for encoding the tissue transporter and the enzyme that incorporates the excess element into bile, generating toxic accumulation in the liver, cornea, and central nervous system. According to his wife, the patient had been treated for an unspecified mood disorder. The clinical picture was characterized by depressive mood, anhedonia, and anxiety. He had his first seizure episode on December 3rd, 2021. He progressed with dysarthria, ataxic gait, dystonia of the right-hand flexor muscles, and intermittent urinary incontinence. Marked worsening was observed after the diagnosis of COVID-19 in February 2022. At the clinical evaluation on March 24th, risorius muscle dystonia (risus sardonicus), resting tremor, and Kayser Fleischer rings at slit-lamp examination was also noted.
Laryssa Garcia de Almeida. 2026. \u201cNeurological Wilson Disease in a Young Brazilian Adult: A Case Report\u201d. Global Journal of Medical Research - A: Neurology & Nervous System GJMR-A Volume 23 (GJMR Volume 23 Issue A3): .
Crossref Journal DOI 10.17406/gjmra
Print ISSN 0975-5888
e-ISSN 2249-4618
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Total Score: 107
Country: Brazil
Subject: Global Journal of Medical Research - A: Neurology & Nervous System
Authors: Laryssa Garcia de Almeida, Ilana Werneck Augsten, Yan da Silva Raposo, Hiago Antunis Silva, Patrícia Marques Mendes, Igor Pereira Matos de Oliveira, Eduardo Mendonça Werneck da Silva (PhD/Dr. count: 0)
View Count (all-time): 173
Total Views (Real + Logic): 1163
Total Downloads (simulated): 12
Publish Date: 2026 01, Fri
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We report a rare case of Wilson’s Disease with neurologic features in a 31-year-old man. This disease consists of a disturbance of copper metabolism secondary to a mutation in the gene responsible for encoding the tissue transporter and the enzyme that incorporates the excess element into bile, generating toxic accumulation in the liver, cornea, and central nervous system. According to his wife, the patient had been treated for an unspecified mood disorder. The clinical picture was characterized by depressive mood, anhedonia, and anxiety. He had his first seizure episode on December 3rd, 2021. He progressed with dysarthria, ataxic gait, dystonia of the right-hand flexor muscles, and intermittent urinary incontinence. Marked worsening was observed after the diagnosis of COVID-19 in February 2022. At the clinical evaluation on March 24th, risorius muscle dystonia (risus sardonicus), resting tremor, and Kayser Fleischer rings at slit-lamp examination was also noted.
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