Internal cervical artery dissection represent a common etiology of stroke in the young, while the most common central nervous system manifestation of Fabry Disease (FD) is acute cerebral ischemia. Nevertheless, internal carotid artery disease has been scarcely associated with Fabry Disease. We describe the neuroimaging findings of an 49-year-old patient presenting with acute left middle cerebral artery occlusion due to an underlying internal carotid artery dissection. The patient was successfully treated with intravenous thrombolysis and mechanical thrombectomy. Further diagnostic work-up revealed bilateral cornea verticillata and large-fiber polyneuropathy with impaired cold and warm perception. Low a-galactosidase levels and molecular g...
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Fabry disease is an inborn error of glycosphingolipid catabolism caused by deficient activity of the...
<div><p>Background and Purpose</p><p>Cerebral autosomal dominant arteriopathy with subcortical infar...
Background and Purpose: Data on the prevalence of Fabry disease in patients with central nervous sys...
Background and Purpose—Data on the prevalence of Fabry disease in patients with central nervous syst...
BACKGROUND AND PURPOSE: Data on the prevalence of Fabry disease in patients with central nervous sys...
International audienceBACKGROUND: Fabry disease (OMIM 301 500) is an X-linked lysosomal storage dise...
Background: Fabry disease (FD) is an X-linked lysosomal storage disorder frequently associated with ...
ObjectiveTo characterize the prevalence of brain ischemia and cerebral small vessel disease in a coh...
Background: TIA and stroke, both ischemic and hemorrhagic, may complicate Fabry disease at young-adu...
BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder frequently associated with ...
Introduction: Fabry disease (FD) is a lysosomal storage disorder associated with marked cerebrovascu...
Fabry's disease is an X-linked lysosomal storage disorder resulting from alpha-galactosidase A defic...
A high load of white matter lesions and enlarged basilar arteries have been shown in selected patien...
Objective: To explore the association between Enzyme Replacement Therapy (ERT), clinical characteris...
The online version of this article, along with updated information and services, is located on th
Fabry disease is an inborn error of glycosphingolipid catabolism caused by deficient activity of the...
<div><p>Background and Purpose</p><p>Cerebral autosomal dominant arteriopathy with subcortical infar...
Background and Purpose: Data on the prevalence of Fabry disease in patients with central nervous sys...
Background and Purpose—Data on the prevalence of Fabry disease in patients with central nervous syst...
BACKGROUND AND PURPOSE: Data on the prevalence of Fabry disease in patients with central nervous sys...
International audienceBACKGROUND: Fabry disease (OMIM 301 500) is an X-linked lysosomal storage dise...
Background: Fabry disease (FD) is an X-linked lysosomal storage disorder frequently associated with ...
ObjectiveTo characterize the prevalence of brain ischemia and cerebral small vessel disease in a coh...
Background: TIA and stroke, both ischemic and hemorrhagic, may complicate Fabry disease at young-adu...
BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder frequently associated with ...
Introduction: Fabry disease (FD) is a lysosomal storage disorder associated with marked cerebrovascu...
Fabry's disease is an X-linked lysosomal storage disorder resulting from alpha-galactosidase A defic...
A high load of white matter lesions and enlarged basilar arteries have been shown in selected patien...
Objective: To explore the association between Enzyme Replacement Therapy (ERT), clinical characteris...
The online version of this article, along with updated information and services, is located on th
Fabry disease is an inborn error of glycosphingolipid catabolism caused by deficient activity of the...
<div><p>Background and Purpose</p><p>Cerebral autosomal dominant arteriopathy with subcortical infar...