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PedAM

Pediatric Disease Annotations & Medicines




Disease ischemic stroke
Phenotype C0002986|fabry disease
Sentences 2
PubMedID- 23168217 Background: a german study diagnosed 4% of young cryptogenic ischemic stroke patients with fabry disease, an x-linked lysosomal storage disease caused by mutations in the alpha-galactosidase a (alpha-gal-a) gene resulting in an accumulation of glycosphingolipids.
PubMedID- 21420783 No other case of thrombolysis for ischemic stroke in fabry disease has been described in the literature.

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