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Subacute sclerosing panencephalitis - current perspectives.

TLDR
Subacute sclerosing panencephalitis is a progressive neurodegenerative disease that usually occurs 7–10 years after measles infection and is preventable by ensuring that an effective vaccine program for measles is made compulsory for all children younger than 5 years in endemic countries.
Abstract
Subacute sclerosing panencephalitis is a progressive neurodegenerative disease. It usually occurs 7–10 years after measles infection. The clinical course is characterized by progressive cognitive decline and behavior changes followed by focal or generalized seizures as well as myoclonus, ataxia, visual disturbance, and later vegetative state, eventually leading to death. It is diagnosed on the basis of Dyken’s criteria. There is no known cure for subacute sclerosing panencephalitis to date, but it is preventable by ensuring that an effective vaccine program for measles is made compulsory for all children younger than 5 years in endemic countries.

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Atypical Pediatric Demyelinating Diseases of the Central Nervous System.

TL;DR: Atypical demyelinating disease may mimic classic neuroinflammatory diseases of the central nervous system and through careful history-taking and review of atypical MRI findings, patients may avoid misdiagnosis and mistreatment.
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Substantial Remission in Subacute Sclerosing Panencephalitis by Following the Ketogenic Diet: A Case Report.

TL;DR: KD has an anti-inflammatory effect and can halt and reverse neurodegenerative changes and its neuroprotective effects could be due to the reduced oxidative stress, enhanced mitochondrial activity, and the suppression of pro-apoptotic factors.
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Measles Induced Encephalitis: Recent Interventions to Overcome the Obstacles Encountered in the Management Amidst the COVID-19 Pandemic

TL;DR: The management of measles-induced encephalitis mainly revolves around prevention against contracting the disease and providing supportive care if acquired as discussed by the authors, which is the major means of preventing this disease in childhood.
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Options in the Treatment of Subacute Sclerosing Panencephalitis: Implications for Low Resource Areas

TL;DR: In this paper , the authors explore the current global status of SSPE, its treatment, and preventive measures, and elucidate on these approaches and their limitations, reasons for poor vaccine coverage in low and middle-income countries, as well as the possible solutions to the prevention of measles and eventual avoidance of sclerosing panencephalitis.
Journal ArticleDOI

Host Cell Restriction Factors of Paramyxoviruses and Pneumoviruses.

TL;DR: An outlook is provided regarding the landscape of emerging technologies and tools available to study host cell restriction factors, as well as the suitability of these proteins as targets for broad-spectrum antiviral therapeutics.
References
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Journal ArticleDOI

Subacute Sclerosing Panencephalitis: More Cases of This Fatal Disease Are Prevented by Measles Immunization than Was Previously Recognized

TL;DR: It was determined that the development of SSPE was associated with the measles resurgence that occurred in the United States during 1989-1991, and the estimated risk of developing S SPE was 10-fold higher than the previous estimate reported for the United United States in 1982.
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Subacute sclerosing panencephalitis: an update.

TL;DR: Management of the disease includes seizure control and avoidance of secondary complications associated with the progressive disability, and trials of treatment with interferon, ribavirin, and isoprinosine using different methodologies have reported beneficial results.
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Review of the effect of measles vaccination on the epidemiology of SSPE

TL;DR: A comprehensive review of the impact of measles immunization on the epidemiology of SSPE and examined epidemiological evidence on whether there was any vaccine-associated risk was conducted in this paper.
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Cellular inclusions in cerebral lesions of epidemic encephalitis: second report

TL;DR: Encephalitis is a term which has been applied to a wide variety of diseases of the central nervous system, and the clinician uses it to designate an obscure, diffuse disease of the brain, whether of proved inflammatory nature or not.
Journal ArticleDOI

Subacute sclerosing panencephalitis.

TL;DR: There is no effective treatment to completely cure SSPE, but Oral isoprinosine and intrathecal or intraventricular alpha-interferon may prolong survival to some extent.
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