CLINICAL, RADIOLOGICAL AND GENETIC ASPECTS OF LEUKODYSTROPHIES

被引：0

作者：

Laszlo, A. ^{[1
]}

Elpeleg, On ^{[2
]}

Horvath, K. ^{[3
]}

Jakobs, C. ^{[4
]}

Kobor, J. ^{[1
]}

Gal, A. ^{[5
]}

Barsi, P. ^{[6
]}

Kelemen, A. ^{[6
]}

Saracz, J. ^{[7
]}

Svekus, A. ^{[8
]}

Tegzes, A. ^{[9
]}

Voeroes, E. ^{[10
]}

机构：

[1] Univ Szeged, Albert Szent Gyorgyi Med Ctr, Dept Pediat, H-6720 Szeged, Koranyi Fasor, Hungary

[2] Shaare Zedek Med Ctr, Metab Disorders Unit, Jerusalem, Israel

[3] Semmelweis Univ, Radiol Clin, H-1085 Budapest, Hungary

[4] Univ Med Ctr, Dept Clin Chem, Metab Unit, Amsterdam, Netherlands

[5] Inst Human Genet, Hamburg Eppendorf, Germany

[6] Semmelweis Univ, Dept Neurol, H-1085 Budapest, Hungary

[7] Pal Heim Hosp, Dept Childs Neurol, Budapest, Hungary

[8] Cty Hosp, Dept Pediat, Gyula, Hungary

[9] Bethesda Hosp, Budapest, Hungary

[10] Univ Szeged, Dept Radiol, Szeged, Hungary

来源：

IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE | 2010年 / 63卷 / 7-8期

关键词：

different types of leukodystrophies; clinical; radiological and genetic aspects; PELIZAEUS-MERZBACHER-DISEASE; MYELIN BASIC-PROTEIN; OLIVOPONTOCEREBELLAR ATROPHY; ALEXANDER-DISEASE; ASPARTOACYLASE GENE; PROTEOLIPID PROTEIN; CANAVAN-DISEASE; MUTATION; DISORDERS; DELETION;

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

The authors summarize the pathomechanism of the myelination process, the clinical, radiological and the genetical aspects of the leukodystrophies, as in 18q deletion syndrome, adrenoleukodysrtophy, metachromatic leukodystrophy, Pelizaeus-Merzbacher leukodystrophy, Alexander disease and olivo-ponto-cerebellar atrophy (OPCA).

引用

页码：266 / 273

页数：8

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