What is Susac syndrome? - A brief review of articles

نویسندگان

  • Ferdos Nazari
  • Amirreza Azimi
  • Siamak Abdi
چکیده

Susac's syndrome (SS) is a clinical triad of encephalopathy, branch retinal artery occlusion and sensorineural hearing loss and maybe due to an immune-mediated endotheliopathy. Because of its rarity and some similarities to other common neurological conditions such as multiple sclerosis and acute disseminated encephalomyelitis, it is often misdiagnosed and therefore mistreated. To the best of our knowledge, there is only one case report from our country with this diagnosis. Here, we have a short discussion on this issue to introduce it to our colleagues and remind it as a differential diagnosis in patients with unexplained encephalopathy.

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A Review Study on Various Conservative Management Strategies for Patellofemoral Pain Syndrome: What Is the Best Intervention?

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گزارش یک مورد سندروم نادر Susac از بخش نورولوژی بیمارستان امام خمینی، سال 1378

This syndrome is a very rare neurological presentation which was first reported by Susac in 1975, and usually involves the young women with triad of: (1) Visual loss due to occlusion of retinal artery branches. (2) Subacute encephalopathy with psychic manifestation, personality disorders, involvement of the cortico-spianal tracts, pseudo-bulbar, focal or generalized seizures and myoclonic jerks...

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Intravitreal Triamcinolone in Susac Syndrome.

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Susac syndrome as an example of a rare vasculopathy.

Susac syndrome is a rare vasculopathy affecting small vessels of the brain, the retina and the cochlea. The pathogenesis of this syndrome is unknown. It is characterized by a triad of clinical symptoms, i.e. encephalopathy, visual disorders and hearing disorders. The aim of this work was to review available data about the clinical course, diagnosis and treatment of Susac syndrome.

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عنوان ژورنال:

دوره 13  شماره 

صفحات  -

تاریخ انتشار 2014