Subacute sclerosing panencephalitis

Semin Pediatr Neurol. 1996 Dec;3(4):260-9. doi: 10.1016/s1071-9091(96)80030-1.

Abstract

Subacute sclerosing panencephalitis (SSPE), a neurodegenerative disease caused by a persistent "slow virus infection" with a mutated measles virus, is endemic in much of the developing world. Its incidence will increase in the USA, not only in immigrants, but also because of the 1988-1990 measles epidemic. This report reviews the pathogenesis, clinical and laboratory diagnosis, and future perspectives in treatment and prevention.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Brain / pathology
  • Child
  • Child, Preschool
  • Defective Viruses / genetics
  • Humans
  • Infant
  • Interferon-alpha / administration & dosage
  • Measles virus / genetics
  • Mutation / genetics
  • Neurologic Examination / drug effects
  • SSPE Virus / genetics
  • Subacute Sclerosing Panencephalitis / diagnosis*
  • Subacute Sclerosing Panencephalitis / therapy
  • Subacute Sclerosing Panencephalitis / virology

Substances

  • Interferon-alpha