| Autor: |
Raut TP; Department of Neurology, CSMMU Lucknow, Lucknow, Uttar Pradesh, India., Singh MK, Garg RK, Naphade PU |
| Jazyk: |
angličtina |
| Zdroj: |
BMJ case reports [BMJ Case Rep] 2012 Dec 14; Vol. 2012. Date of Electronic Publication: 2012 Dec 14. |
| DOI: |
10.1136/bcr-2012-006764 |
| Abstrakt: |
Subacute sclerosing panencephalitis (SSPE) is a slowly progressing inflammatory and degenerative disorder of the brain caused by a mutant measles virus. The diagnosis of SSPE is based on characteristic clinical and EEG findings (periodic complexes) and demonstration of elevated antibody titres against measles in cerebrospinal fluid. SSPE can have atypical clinical features at the onset. The authors here report a case of a 3-year-old child who presented with vision loss followed 15 months later by quadriparesis with bladder involvement. These clinical features resembled that of neuromyelitis optica. However, as the disease progressed, appearance of myoclonic jerks, periodic discharges on EEG and positive cerebrospinal fluid serology for measles led to the final diagnosis of SSPE. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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