Acute post-)infective polyneuritis
Miller Fisher Syndrome
Acute infective polyneuritis
Acute inflammatory demyelinating polyneuropathy
Fisher’s syndrome
Guillain barre syndrome
Guillain-barrè syndrome
Miller fischer variant of guillain barre syndrome
Polyneuritis, acute infectious
Polyneuropathy multiple nerve disorder)
A variant of the guillain-barre syndrome characterized by the acute onset of oculomotor dysfunction, ataxia, and loss of deep tendon reflexes with relative sparing of strength in the extremities and trunk. The ataxia is produced by peripheral sensory nerve dysfunction and not by cerebellar injury. Facial weakness and sensory loss may also occur. The process is mediated by autoantibodies directed against a component of myelin found in peripheral nerves. Adams et al., Principles of Neurology, 6th ed, p1313; neurology 1987 sep;37 9):1493-8)
An acute inflammatory autoimmune neuritis caused by t cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. from Adams et al., Principles of Neurology, 6th ed, pp1312-1314)
An acute, autoimmune inflammatory process affecting the peripheral nervous system and nerve roots. It results in demyelination. It is often caused by an acute viral or bacterial infection.
Guillain-barre syndrome is a rare disorder that causes your immune system to attack your peripheral nervous system pns). The pns nerves connect your brain and spinal cord with the rest of your body. Damage to these nerves makes it hard for them to transmit signals. As a result, your muscles have trouble responding to your brain. No one knows what causes the syndrome. Sometimes it is triggered by an infection, surgery or a vaccination. The first symptom is usually weakness or a tingling feeling in your legs. The feeling can spread to your upper body. In severe cases, you become almost paralyzed. This is life-threatening. You might need a respirator to breathe. Symptoms usually worsen over a period of weeks, then stabilize. Most people recover. Recovery can take a few weeks to a few years. Treatment options during the symptom period include medicines or a procedure called plasma exchange.
Progressive ascending motor neuron paralysis of unknown etiology, frequently following an enteric or respiratory infection.
G61.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM G61.0 became effective on October 1, 2022.
This is the American ICD-10-CM version of G61.0 – other international versions of ICD-10 G61.0 may differ.