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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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Who first discovered WAGR syndrome?
WAGR syndrome was first described by Dr. Rudy WAGR, who noticed a pattern of symptoms in four children who had similar characteristics. The syndrome was later named after the initials of the symptoms it encompasses (Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation).
What are the key differences between Klinefelter syndrome and Turner syndrome?
Klinefelter syndrome is a genetic condition in males where they have an extra X chromosome, resulting in symptoms like infertility and low testosterone levels. Turner syndrome, on the other hand, is a genetic condition in females where they are missing part or all of one of their X chromosomes, leading to symptoms like short stature and infertility.
How long does stickler syndrome last?
Stickler syndrome is a genetic disorder that is present from birth and persists throughout a person's life. The symptoms and severity of the condition can vary widely among individuals, but the genetic mutation that causes Stickler syndrome is lifelong. Treatment is focused on managing symptoms and complications associated with the syndrome.
Who discovered Jacobsen Syndrome?
Jacob's Syndrome, or XYY Syndrome was first discovered by cytogeneticists Joe Hin Tjio and Albert Levan.
Are there any celebs with stickler syndrome?
Yes, actress Bella Thorne has been open about her diagnosis of Stickler syndrome. Stickler syndrome is a rare genetic disorder that affects connective tissues in the body, leading to various symptoms such as joint problems, vision issues, and facial features characteristic of the syndrome.
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.
Who first discovered WAGR syndrome?
WAGR syndrome was first described by Dr. Rudy WAGR, who noticed a pattern of symptoms in four children who had similar characteristics. The syndrome was later named after the initials of the symptoms it encompasses (Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation).
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).
What are the symptoms of Cri Du chat syndrome?
See cri-du-chat-syndrome-causes-and-symptoms
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.
What are the symptoms of Cinderella syndrome?
The symptoms of Cinderella syndrome are only usually listed as false accusations from the adopted children toward their adoptive stepmother. There are no other symptoms.
What are symptoms of keppel trewlawney weber syndrome?
what is kepel weber syndrome
