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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease hunter syndrome
Comorbidity C0007682|cns disease
Sentences 2
PubMedID- 25836678 In addition, the long residence time of i2s in the csf after it administration should provide the time needed for the i2s to penetrate the brain tissue and degrade the accumulated glycosaminoglycans, which may have an impact on the progression of cns disease manifestations in patients with hunter syndrome.
PubMedID- 21225451 These suggest that developing a cure for the cns diseases of mps iiib and other similar disorders may require more than the simple restoration of the absent or deficient lysosomal enzyme activity.

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