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1.
Zh Nevrol Psikhiatr Im S S Korsakova ; 124(4. Vyp. 2): 72-76, 2024.
Artículo en Ruso | MEDLINE | ID: mdl-38696154

RESUMEN

The prevalence of cognitive impairment is steadily increasing compared to previous years. According to the World Health Organization, the number of people living with dementia will increase reaching 82 million in 2030 and 152 million in 2050. The most common cause is Alzheimer's disease (AD). The pathophysiological process in AD begins several years before the onset of clinical symptoms; so identifying it at an early stage would likely improve the clinical prognosis. The article presents EEG changes in patients with AD, and discusses the possibility of using EEG as a screening method for examining patients with cognitive impairment.


Asunto(s)
Enfermedad de Alzheimer , Electroencefalografía , Enfermedad de Alzheimer/fisiopatología , Enfermedad de Alzheimer/diagnóstico , Humanos , Encéfalo/fisiopatología , Disfunción Cognitiva/fisiopatología , Disfunción Cognitiva/etiología , Disfunción Cognitiva/diagnóstico , Pronóstico
2.
Artículo en Ruso | MEDLINE | ID: mdl-36719116

RESUMEN

Patients with epilepsy who have also hearing loss represent a distinct group of patients, often with aggravated medical history, comorbidities and high potential for disability. The etiopathogenetic factors of epilepsy and hearing loss may be common to these conditions (neuroinfections, craniocerebral injuries, cerebral circulatory disorders, perinatal pathology, etc.). In addition, these two syndromes may occur as part of hereditary diseases, so their timely recognition and genetic diagnosis are important for determining further medical and genetic prognosis. This article provides an overview of orphan genetic diseases associated with epilepsy and hearing loss - MERRF syndrome, MELAS syndrome, EAST syndrome, Ayme-Grippsyndrome, epilepsy, hearing loss and mental retardation syndromes, associated with mutations in SPATA5 gene, DOOR syndrome, Gustavson syndrome.


Asunto(s)
Sordera , Epilepsia , Síndromes Epilépticos , Pérdida Auditiva Sensorineural , Pérdida Auditiva , Humanos , Sordera/genética , Epilepsia/complicaciones , Epilepsia/diagnóstico , Epilepsia/genética , Pérdida Auditiva/etiología , Pérdida Auditiva/genética , Mutación
3.
Artículo en Ruso | MEDLINE | ID: mdl-36168683

RESUMEN

Based on the available literature data, the article discusses the prevalence of various forms of damage of the peripheral nervous system in COVID-19 and in the post-COVID period. Information about the clinical features and the course of individual cranial neuropathies, chronic dysimmune neuropathies, Guillain-Barré syndrome, drug-induced neuropathies, fine fiber neuropathy, myasthenia gravis and polyneuropathy of critical conditions was systemized in the context of coronavirus infection. SARS-CoV-2 can trigger various stages of pathogenesis, including neuroimmune ones, which cause long-term consequences of COVID-19, including those associated with the damage of the peripheral nervous system. Awareness of COVID-19-associated pathological conditions will allow assessment of the possible risks of damage of the peripheral nervous system, recognize them at early stages and develop more effective approaches for treatment.


Asunto(s)
COVID-19 , Síndrome de Guillain-Barré , Miastenia Gravis , COVID-19/complicaciones , Síndrome de Guillain-Barré/complicaciones , Síndrome de Guillain-Barré/etiología , Humanos , Miastenia Gravis/complicaciones , Sistema Nervioso Periférico , SARS-CoV-2
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