Mucopolysaccharidosis (MPS) is a group of metabolic disorders caused by the deficiency or complete absence certain lysosomal enzymes responsible for breakdown mucopolysaccharides, causing an accumulation glycosaminoglycans (GAGs) throughout body. type I (MPS I), also called Hurler syndrome, autosomal recessive storage disorder resulting from enzyme α-L-iduronidase. This report aims to present c...

The mucopolysaccharidosis (MPS) type VI is a rare lysosomal storage disease presenting leukocyte inclusions (Alder-Reilly anomaly) and lymphocytes with metachromatic inclusion surrounded by clear spaces, Gasser cells. Currently, an enzyme replacement therapy (ERT) galsulfase used to treat MPS VI. This study evaluated 14 patients performed cell counts before after six months from the beginning o...

The thesis based on the case study of “San Yue Jie” Festival of Bai Nationality, reavealed the history, developing process and current situation of “San Yue Jie” Festival. Considered that the festival acted as an important role in the manority culture, the festival economy was a key to develop the manority culture. Futher more, the thesis disclosed the positive influences, formation and feature...