Literature DB >> 20300124

Cerebral hemorrhage in Fabry's disease.

Katsuya Nakamura1, Yoshiki Sekijima, Kimitoshi Nakamura, Kiyoko Hattori, Kiyoshiro Nagamatsu, Yusaku Shimizu, Takuji Yasude, Masao Ushiyama, Fumio Endo, Yoshimitsu Fukushima, Shu-ichi Ikeda.   

Abstract

Fabry's disease is an X-linked lysosomal storage disorder resulting from alpha-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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Year:  2010        PMID: 20300124     DOI: 10.1038/jhg.2010.18

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  5 in total

Review 1.  Neurocutaneous Disorders for the Practicing Neurologist: a Focused Review.

Authors:  Anna Carolina Paiva Costa T Figueiredo; Nikolas Mata-Machado; Matthew McCoyd; José Biller
Journal:  Curr Neurol Neurosci Rep       Date:  2016-02       Impact factor: 5.081

2.  Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients.

Authors:  Kiyoshiro Nagamatsu; Yoshiki Sekijima; Katsuya Nakamura; Kimitoshi Nakamura; Kiyoko Hattori; Masao Ota; Yusaku Shimizu; Fumio Endo; Shu-Ichi Ikeda
Journal:  J Hum Genet       Date:  2017-03-09       Impact factor: 3.172

3.  Lessons from everyday stroke care for clinical research and vice versa: comparison of a comprehensive and a research population of young stroke patients.

Authors:  Christian Tanislav; Ulrike Grittner; Bjoern Misselwitz; Gerhard Jan Jungehuelsing; Christian Enzinger; Bettina von Sarnowski; Jukka Putaala; Manfred Kaps; Peter Kropp; Arndt Rolfs; Turgut Tatlisumak; Franz Fazekas; Edwin Kolodny; Bo Norrving
Journal:  BMC Neurol       Date:  2014-03-07       Impact factor: 2.474

4.  A new mutation found in newborn screening for Fabry disease evaluated by plasma globotriaosylsphingosine levels.

Authors:  Yasutsugu Chinen; Sadao Nakamura; Tomohide Yoshida; Hiroki Maruyama; Kimitoshi Nakamura
Journal:  Hum Genome Var       Date:  2017-02-16

5.  A Case of Cerebral Aneurysmal Subarachnoid Hemorrhage in Fabry's Disease.

Authors:  Youn Hyuk Chang; Sung-Kyun Hwang
Journal:  J Korean Neurosurg Soc       Date:  2013-03-31
  5 in total

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