A RARE CASE OF HUNTER SYNDROME – CASE REPORT

A RARE CASE OF HUNTER SYNDROME – CASE REPORT

Mucopolysaccharidoses (MPSs) are a group of rare genetic disorders within the larger family of lysosomal diseases. MPSs disorders are caused by a defi ciency in the activity of a specifi c lysosomal enzyme required for the degradation of glycosaminoglycans (GAGs). MPS type II, also called Hunter s...

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Bibliographic Details
Main Authors: Lorena Elena Melit, Oana Marginean, Carmen Duicu, Cristina Campean, Maria Oana Marginean
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2015-03-01
Series:Romanian Journal of Pediatrics
Subjects:
hunter syndrome
child
Online Access:https://revistemedicale.amaltea.ro/Romanian_Journal_of_PEDIATRICS/Revista_Romana_de_PEDIATRIE-2015-Nr.1/EN/RJP_2015_1_EN_Art-08.pdf

Internet

https://revistemedicale.amaltea.ro/Romanian_Journal_of_PEDIATRICS/Revista_Romana_de_PEDIATRIE-2015-Nr.1/EN/RJP_2015_1_EN_Art-08.pdf

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