Acute disseminated encephalomyelitis
encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin

Acute disseminated encephalomyelitis (ADEM), or acute demyelinating encephalomyelitis, is a rare autoimmune disease marked by a sudden, widespread attack of inflammation in the brain and spinal cord. As well as causing the brain and spinal cord to become inflamed, ADEM also attacks the nerves of the central nervous system and damages their myelin insulation, which, as a result, destroys the white matter. The cause is often a trigger such as from viral infection or, in extraordinarily rare cases, vaccinations.
ADEM's symptoms resemble those of multiple sclerosis (MS), so the disease itself is sorted into the classification of the multiple sclerosis borderline diseases. However, ADEM has several features that distinguish it from MS. Unlike MS, ADEM occurs usually in children and is marked with rapid fever, although adolescents and adults can get the disease too. ADEM consists of a single flare-up, whereas MS is marked with several flare-ups (or relapses) over a long period of time. Relapses following ADEM are reported in up to a quarter of patients. However, the majority of these 'multiphasic' presentations following ADEM likely represent MS. ADEM is also distinguished by a loss of consciousness, coma and death, which is very rare in MS, except in severe cases.
It affects about 8 per 1,000,000 people per year. Although it occurs in all ages, most reported cases are in children and adolescents, with the average age around 5 to 8 years old.
“Acute disseminated encephalomyelitis” enters the record as encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin. Crown Archives preserves that source wording while asking what Acute, disseminated and encephalomyelitis can confirm, complicate or overturn.
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