Laronidase

Category: Genetic Disorders



Laronidase Overview

Iduronidase (EC 3.2.1.76, L-iduronidase, alpha-L-iduronidase, laronidase), sold as Aldurazyme, is an enzyme with the systematic name glycosaminoglycan alpha-L-iduronohydrolase.[3][4][5] This enzyme catalyses the hydrolysis of unsulfated alpha-L-iduronosidic linkages in dermatan sulfate.[6] It is a glycoprotein enzyme found in the lysosomes of cells. It is involved in the degeneration of glycosaminoglycans such as dermatan sulfate...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Iduronidase

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Possible Dosages for this and Related Drugs:

Laronidase
  • Solution: 2.9mg/5ml
  • Vial: 2.9mg/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

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