Cerebral hemorrhage in Fabry's disease

被引:0
作者
Katsuya Nakamura
Yoshiki Sekijima
Kimitoshi Nakamura
Kiyoko Hattori
Kiyoshiro Nagamatsu
Yusaku Shimizu
Takuji Yasude
Masao Ushiyama
Fumio Endo
Yoshimitsu Fukushima
Shu-ichi Ikeda
机构
[1] Shinshu University School of Medicine,Department of Medicine (Neurology and Rheumatology)
[2] Shinshu University Hospital,Division of Clinical and Molecular Genetics
[3] Graduate School of Medical Science,Department of Pediatrics
[4] Kumamoto University,Department of Neurology
[5] Ina Central Hospital,Department of Neurology
[6] Hokushin General Hospital,Department of Neurology
[7] Kenwakai Hospital,undefined
来源
Journal of Human Genetics | 2010年 / 55卷
关键词
α-galactosidase A; Fabry's disease; cerebral hemorrhage; cerebral infarction; stroke;
D O I
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中图分类号
学科分类号
摘要
Fabry's disease is an X-linked lysosomal storage disorder resulting from α-galactosidase A deficiency. Although ischemic stroke is recognized as an important manifestation of Fabry's disease, hemorrhagic stroke is considered to be rare. Here, we report our recent clinical experience with three hemizygous male patients with Fabry's disease who developed cerebral hemorrhage. One patient had classic type Fabry's disease with p.Ala37Val mutation and others had cerebrovascular variant with p.Glu66Gln mutation. Degeneration of the cerebral small arteries secondary to deposition of glycosphingolipids and aging, in addition to hypertension and antiplatelet/anticoagulant agents, are considered to be contributing factors for hemorrhage. Fabry's disease is frequently associated with not only ischemic but also hemorrhagic stroke, especially in elderly patients.
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页码:259 / 261
页数:2
相关论文
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