نتایج جستجو برای: leukodystrophy
تعداد نتایج: 2650 فیلتر نتایج به سال:
Cardiomyopathy and leukodystrophy are life-threatening complications of multiple acyl-CoA dehydrogenase deficiency (MADD). A 2-year-old boy with this disorder developed rapidly progressive leukodystrophy resulting in complete paralysis within 4 months. Within a week of starting sodium-D,L-3-hydroxybutyrate he had improved. After 2 years, neurological function returned, including walking indepen...
how to cite this article: shalbafan b. alexander and canavan disease. iran j child neurol. autumn 2014;8;4(suppl.1):20-21.
Alexander disease is a rare autosomal recessive disorder that is characterized by degeneration of the white matter in the central nervous system. Alexander disease is a leukodystrophy that is usually observed in early childhood but rarely in adults. It is characterized by megalencephaly, demyelinization and multiple Rosenthal fibers. Specific magnetic resonance imaging (MRI) findings and geneti...
how to cite this article: taghdiri mm. adreno leukodystrophy. iran j child neurol. autumn 2014;8;4(suppl.1):13. pls see pdf.
how to cite this article: jabbehdari s, rahimian e, jafari n, sanii s, khayatzadeh kakhki s, nejad biglari h. the clinical features and diagnosis of metachromatic leukodystrophy: a case series of iranian pediatric patients. iran j child neurol. summer 2015;9(3):57-61. abstract objective metachromatic leukodystrophy disorder (mld) is one of the rare neurometabolic diseases caused due to lack of ...
how to cite this article: ghofrani m. an overview of leukodystrophy (ld). iran j child neurol. autumn 2014; 8:4(suppl. 1):1-2. pls see pdf.
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید