Hunter syndrome, or mucopolysaccharidosis type II, is a rare X-linked disorder caused by a deficiency in the lysosomal enzyme iduronate-2-sulfatase. This results in accumulation of glycosaminoglycans (GAGs) in the lysosomes of various tissues. It causes physical and mental degeneration, in severe cases, death during the teenage years. Dental complications include enamel hypoplasia, microdontia, dentigerous cyst-like follicles, unerupted dentition, malocclusions, gingival hyperplasia, macroglossia, and condylar defects. This is a case report of a 9-year-old boy who visited the Dentistry Department of Pediatric Dentistry, Yonsei University Dental Hospital with a chief complaint of over-all dental treatment and bruxism. This report discusses o...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...
WOS: 000237068400013PubMed ID: 16632276Maroteaux-Lamy syndrome is one of the genetic disorders invol...
Hunter's Syndrome or mucopolysaccharidosis Type II is a rare metabolic disorder caused by the defici...
Hunter syndrome is a lysosomal disease characterized by deficiency of the lysosomal enzyme iduronate...
Hunter syndrome is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronat...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...
Hunter syndrome or mucopolysaccharidosis (MPS) type II is an X-linked recessive disorder caused by a...
Background. This clinical case of orphan disease can be interesting for its early diagnostics which ...
Hunters disease is a rare genetic disorder caused by the abnormal buildup of compounds called glycoa...
Hunter syndrome is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme i...
This review aims to provide clinicians in Latin America with the most current information on the cli...
This review aims to provide clinicians in Latin America with the most current information on the cli...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused ...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare X-linked lysosomal storage disease...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...
WOS: 000237068400013PubMed ID: 16632276Maroteaux-Lamy syndrome is one of the genetic disorders invol...
Hunter's Syndrome or mucopolysaccharidosis Type II is a rare metabolic disorder caused by the defici...
Hunter syndrome is a lysosomal disease characterized by deficiency of the lysosomal enzyme iduronate...
Hunter syndrome is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronat...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...
Hunter syndrome or mucopolysaccharidosis (MPS) type II is an X-linked recessive disorder caused by a...
Background. This clinical case of orphan disease can be interesting for its early diagnostics which ...
Hunters disease is a rare genetic disorder caused by the abnormal buildup of compounds called glycoa...
Hunter syndrome is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme i...
This review aims to provide clinicians in Latin America with the most current information on the cli...
This review aims to provide clinicians in Latin America with the most current information on the cli...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused ...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare X-linked lysosomal storage disease...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...
WOS: 000237068400013PubMed ID: 16632276Maroteaux-Lamy syndrome is one of the genetic disorders invol...