Encephalomyelopolyradiculoneuritis

Encephalomyelopolyradiculoneuritis is a rare disease that is a combination of inflammation of the brain and spinal cord (encephalitis and myelitis) with inflammation of multiple peripheral nerve roots (polyradiculoneuritis).

The disease is characterized by an acute onset with fever, headaches, vomiting, disturbances of consciousness, progressive paresis and paralysis of the limbs, and sensitivity disorders. The causes of encephalomyelopolyradiculoneuritis can be infectious (viral, bacterial) or autoimmune. Diagnosis is based on the clinical picture, lumbar puncture data, MRI of the brain and spinal cord, and nerve conduction studies. Treatment is primarily aimed at fighting infection and inflammation. The prognosis for encephalomyelopolyradiculoneuritis varies from complete recovery to death.

Encephalomyelopolyradiculoneuralgic infection is a chronic disease of the nervous system. Together, these components are diagnosed when doctors identify blood clots in many small blood vessels that ischemia the nervous tissue, which leads to its gradual death. Encephalitolmidpolyradicomatolneuralgiccalgenitalumpolyradicalneuralgia: what are the symptoms and causes of this disease. The pathology is characterized by inflammatory processes in the spinal cord and brain, as well as in peripheral nerve fibers. Damage occurs to the meninges, optic nerve, and cranial nerves. In most cases, the disease progresses without scarring. Main clinical manifestation