نتایج جستجو برای: leukodystrophy

تعداد نتایج: 2650  

Journal: :Journal of neurology, neurosurgery, and psychiatry 1991
M Phelps J Aicardi M T Vanier

Four cases of late-onset Krabbe's leukodystrophy had varying clinical features. One sibling became wheelchair-bound while another leads an active working life. The computed tomography (CT) scan of a third patient showed occipital demyelination with contrast enhancement identical to that seen in an adrenoleucodystrophy. The fourth was the only patient with peripheral neuropathy. All patients had...

Journal: :AJNR. American journal of neuroradiology 2000
M Topçu I Saatci R A Apak F Söylemezoglu Z Akçören

We report unusual MR serial imaging and electron microscopy findings in a 3-year-old boy who had Leigh syndrome with cytochrome-c oxidase (cox) deficiency. The MR imaging findings included periventricular white matter involvement, posteroanterior progression, and extension through the corpus callosum and internal capsule; however, no basal ganglia or brain stem abnormality was found, which was ...

Journal: :The Turkish journal of pediatrics 2010
Uluç Yiş Gert C Scheper Nedret Uran Aycan Unalp Handan Cakmakçi Semra Hiz-Kurul Eray Dirik Marjo S van der Knaap

Megalencephalic leukoencephalopathy with subcortical cysts is a rare leukodystrophy that is characterized by macrocephaly and a slowly progressive clinical course. It is one of the most commonly reported leukoencephalopathies in Turkey. Mutations in the MLC1 gene are the main cause of the disease. We report two patients with megalencephalic leukoencephalopathy with subcortical cysts with confir...

2017
Yuki Miyamoto Tomohiro Torii Kazuko Kawahara Nanami Hasegawa Akito Tanoue Yoichi Seki Takako Morimoto Megumi Funakoshi-Tago Hiroomi Tamura Keiichi Homma Masahiro Yamamoto Junji Yamauchi

Hypomyelinating leukodystrophy (HLD) is genetic demyelinating or dysmyelinating disease and is associated with at least 13 responsible genes. The mutations seem likely cause the functional deficiency of their gene products. HLD4- and HLD5-associated HSPD1 and FAM126A mutations affect biochemical properties of the gene products (Miyamoto et al. (2015,2014) [[1], [2]]). Herein we provide the data...

2013
Mitra Assadi Dah-Jyuu Wang Yadira Velazquez-Rodriquez Paola Leone

Metachromatic leukodystrophy (MLD) is characterized by the accumulation of sulfatide sphingolipids in the brain and peripheral nerves. We report metabolite alterations recorded using multi-voxel proton spectroscopy of the brain in four children with MLD. The data revealed elevated myoinositol/creatine and lactate/creatine ratios as well as decreased N-acetyl aspartate/creatine ratios. We propos...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید