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.

Cervical myelopathy



Total: 1

                      


(per page)
PMID (PMCID)
2118851
MALE Adult
[Cervical myelopathy in mucopolysaccharidosis type II (Hunter's syndrome). Neuroradiologic, clinical and histopathologic findings].
Kaendler S, Bockenheimer S, Grafin Vitzthum H, Galow W.
Dtsch Med Wochenschr. 1990;115(36):1348-52.
[Cervical myelopathy in mucopolysaccharidosis type II (Hunter's syndrome).