Kearns-Sayre Syndrome: Case ReportBabürhan GÜLDİKEN1, Ufuk UTKU1, Ersin TAN2, Nurgül AYDIN1 1Trakya Üniversitesi Tıp Fakültesi Nöroloji ABD 2Hacettepe Üniverersitesi Tıp Fakültesi, Nöroloji Anabilim Dalı, ANKARA
The mitochondrial encephalomyopathies caused by a disorder in the mitochondrial DNAstructure are rare multisystem diseases. MERRF (myoclonic epilepsi, ragged-red fibers),MELAS ( mitochondrial ensefalomyopathy, lactic acidosis, stroke-like episodes) and KSS(kearus-Sayre Syndrome) are the well known mitochondrial encepbalomyopathies. Thereare limited reports about their neuroradiological findings. In Kearns-Sayre Syndrome hasalganglionic calcifications are often seen in CT, but only in a few case reports hyperintenslesions in the brain stem, cerebellum and diencephalic stuctures on T2- weighted MR images are demonstrated. In this study we discussed a KSS patient with his clinical, MRI and pathological findings. Keywords: Kearns-Sayre Syndrome - MRl - CT
Babürhan GÜLDİKEN, Ufuk UTKU, Ersin TAN, Nurgül AYDIN. Kearns-Sayre Syndrome: Case Report. Turk J Neurol. 1995; 1(1): 32-35
Corresponding Author: Babürhan GÜLDİKEN |
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