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is a rare variant of GBS and manifests as a descending paralysis, proceeding in the reverse order of the more common form of GBS. It usually affects the ocular muscles first and presents with the triad of ophthalmoplegia, ataxia, and areflexia. Anti-GQ1b antibodies are present in 90% of cases

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Q: What are the Symptoms of miller fisher syndrome?
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Related questions

Is Miller Fisher Syndrome contagious?

no


What is the recovery period from Fisher's syndrome?

Once Fisher syndrome is identified, treatment can lead to recovery in as soon as two to four weeks after the symptoms are initially acquired.


When was Miller Fisher born?

Miller Fisher was born in 1913.


What is fisher disease?

Most frequently referred to by Miller Fisher Syndrome, it is an acquired disease regarded as a variant of Guillain-Barre syndrome. Abnormal muscle coordination, paralysis of the eye muscles and absence of tendon reflexes are indicators.


Where does Fisher syndrome begin?

Fisher syndrome, on the other hand, begins in the head (paralysis of the eyes) and moves in the direction toward the neck and arms.


What is Fisher syndrome?

Fisher syndrome is a rare, acute neurological disorder characterized by a triad of clinical manifestations that includes brain-damage associated abnormal coordination (ataxia).


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What is the medical term meaning Signs and symptoms that occur together?

syndrome.SYNDROME means Group of symptoms


How is Fisher syndrome treated?

Treatment for Fisher syndrome involves removing the plasma from affected individuals, a procedure called plasmapheresis. In doing so, antibodies that cause the disease are also removed.


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What are symptoms of keppel trewlawney weber syndrome?

what is kepel weber syndrome


What do you call a set of symptoms?

Syndrome