A Rare Case of Hunter Syndrome – Case Report

@inproceedings{Meli2015ARC,
  title={A Rare Case of Hunter Syndrome – Case Report},
  author={Lorena Elena Meliț and Oana Cristina Mărginean and Carmen Duicu and Cristina Campean and Maria Oana Mărginean},
  year={2015}
}
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 syndrome consists in a defi ciency of an enzyme, iduronate-2… CONTINUE READING