subacute sclerosing panencephalitis Antonyms
No Synonyms and anytonyms found
Meaning of subacute sclerosing panencephalitis
subacute sclerosing panencephalitis (n)
a rare chronic progressive encephalitis caused by the measles virus and occurring primarily in children and young adults; death usually occurs within three years; characterized by primary measles infection before the age of two years
subacute sclerosing panencephalitis Sentence Examples
- Subacute sclerosing panencephalitis (SSPE) is a rare but fatal neurological disorder that typically develops in children.
- SSPE is caused by a persistent infection with the measles virus that can remain dormant within the nervous system for years.
- The onset of SSPE is often gradual, but the progression can be rapid, leading to severe disability and death within months.
- The symptoms of SSPE include intellectual decline, behavioral changes, muscular rigidity, and seizures.
- The diagnosis of SSPE is based on clinical presentation, laboratory tests, and brain imaging studies.
- Treatment for SSPE is supportive and may include anticonvulsants, neuroleptics, and rehabilitation therapy.
- The prognosis for SSPE is poor, with most patients dying within a few years of diagnosis.
- The incidence of SSPE has decreased significantly due to widespread vaccination against measles.
- However, cases of SSPE can still occur in those who were not vaccinated or who had an incomplete immune response to the vaccine.
- Researchers are investigating new treatments for SSPE, including antiviral therapies and gene therapy.
FAQs About the word subacute sclerosing panencephalitis
a rare chronic progressive encephalitis caused by the measles virus and occurring primarily in children and young adults; death usually occurs within three year
No synonyms found.
No antonyms found.
Subacute sclerosing panencephalitis (SSPE) is a rare but fatal neurological disorder that typically develops in children.
SSPE is caused by a persistent infection with the measles virus that can remain dormant within the nervous system for years.
The onset of SSPE is often gradual, but the progression can be rapid, leading to severe disability and death within months.
The symptoms of SSPE include intellectual decline, behavioral changes, muscular rigidity, and seizures.
