Mucopolysaccharidosis type 2

A lysosomal storage disease with multisystemic involvement leading to a massive accumulation of glycosaminoglycans and a wide variety of symptoms including distinctive coarse facial features, short stature, cardio-respiratory involvement and skeletal abnormalities. It manifests as a continuum varying from a severe form with neurodegeneration to an attenuated form without neuronal involvement.

Ischemic stroke



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PMID (PMCID)
17056260
MALE Adult
Cerebral infarction in Hunter syndrome.
Neely J, Carpenter J, Hsu W, Jordan L, Restrepo L.
J Clin Neurosci. 2006;13(10):1054-7.
We conclude that ischemic stroke secondary to cardioembolization is a potential complication of Hunter syndrome.