Browsing by Author "Deda, G"
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Combined genetic defects in a child with ischemic stroke: Case report
Deda, G; Icagasioglu, D; Caksen, H; Akar, N (SAGE PUBLICATIONS INC, 2002)A 10-year-old Turkish boy was admitted with mild right spastic hemiplegia. First, he experienced sudden numbness and weakness in the right extremities at the age of 2 years and was diagnosed with right hemiparesis. His ... -
Psychotic disorder in a case with Hallervorden-Spatz disease
Oner, O; Oner, P; Deda, G; Icagasioglu, D (BLACKWELL MUNKSGAARD, 2003)Objective: Hallervorden - Spatz disease is a rare autosomal recessive condition, with early onset of predominantly extrapyramidal dysfunction. The symptoms of the disease are dystonia, rigidity, choreoathetosis, pyramidal ...