Number of the records: 1
panencefalitída subakútna sklerotizujúca
Record number d013344 Date 06.06.2025 Type M - MESH Topical term panencefalitída subakútna sklerotizujúca Other term English (Pseudonym) Encephalitis, Inclusion Body, Measles
English (Pseudonym) Leukoencephalitis, Subacute Sclerosing
English (Pseudonym) Measles Inclusion Body Encephalitis
English (Pseudonym) Panencephalitis, Subacute Sclerosing
English (Pseudonym) SSPE
English (Pseudonym) Van Bogaert's Leukoencephalitis
Slovak (Pseudonym) encefalitída spôsobená inklúznymi telieskami vírusu osýpok
Slovak (Pseudonym) leukoencefalitída sklerotizujúca subakútna
Slovak (Pseudonym) SSPE
Slovak (Pseudonym) van Bogaertova leukoencefalitída
Slovak (Pseudonym) leukoencefalitída subakútna sklerotizujúca
Slovak (Pseudonym) encefalitída osýpková s výskytom inkluzívnych teliesok
Slovak (Pseudonym) panencefalitída subakútna sklerotizujúca
Slovak (Pseudonym) leucoencephalitis sclerotisans subacuta
See also (Later heading) vírus osýpok
UDC C01.207.245.340.600C01.207.399.750.600C01.925.182.525.600C01.925.782.580.600.500.500.800C01.925.839.862C10.228.140.430.520.750.600C10.228.228.245.340.600C10.228.228.399.750.600C10.586.250.520.750.600 Note A rare, slowly progressive encephalitis caused by chronic infection with the MEASLES VIRUS. The condition occurs primarily in children and young adults, approximately 2-8 years after the initial infection. A gradual decline in intellectual abilities and behavioral alterations are followed by progressive MYOCLONUS; MUSCLE SPASTICITY; SEIZURES; DEMENTIA; autonomic dysfunction; and ATAXIA. DEATH usually occurs 1-3 years after disease onset. Pathologic features include perivascular cuffing, eosinophilic cytoplasmic inclusions, neurophagia, and fibrous gliosis. It is caused by the SSPE virus, which is a defective variant of MEASLES VIRUS. (From Adams et al., Principles of Neurology, 6th ed, pp767-8) 
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Number of the records: 1