Vogt-Koyanagi-Harada Syndrome With Severe Neurologic Impairment
Journal Title: Journal of Neurological Sciences-Turkish - Year 2009, Vol 26, Issue 2
Abstract
Vogt-Koyanagi-Harada (VKH) syndrome is a rare systemic disease involving various melanocyt-containing organs with subacute chronic course. Bilateral uveitis associated with cutaneous, neurological and auditory abnormalities characterizes this syndrome. The degree of neurological symptoms may vary but they are usually mild. Here we report an unusual case with severe visual and neurological impairment such as bilateral amaurosis, recurrent status epilepticus episodes and progressive mental changes.
Authors and Affiliations
Tolga OZDEMIRKIRAN, Filiz SAGTAS, Mehmet CELEBISOY, Sehnaz ARICI, Figen TOKUCOGLU
Kültüre Edilmiş Glioblastoma Multiforme Hücrelerinin Morfolojisi
Bu çalışmanın amacı, beş hastadan elde edilen ve kültürü yapılan glioblastoma multiforme hücrelerinin morfolojisini değerlendirmektir. Yapılan malign astrositom doku kültür hücreleri fenotipik olarak polimorfik karakter...
Deep Cerebral Venous Thrombosis In Adults
As the thrombosis of deep cerebral venous system is rare and usually fatal in adults, we present three cases, two of which had excellent prognosis. Cranial CT scan shows increased density along the course of the vein of...
Temporosfenoidal Fibröz Displazi: Olgu Sunumu
Fibröz displazi, kemiklerde değişikliklere neden olan kemiklerin lokal hastalıklarıdır. Biz, temporosfenoidal kemiğin fibröz displazi olgusunu sunduk. Bu vakada, kafa tabanına kadar uzanan temporal kemik parçasını subtot...
Medicine in Stamps Alois Alzheimer: the Father of Alzheimer Disease
During the times of World War I, Germany was an important pioneer in many areas of science and medicine. Alois Alzheimer, who lived during this period, was one of the founders of the field of neuropathology. He described...
Serebral sinüs trombozu