We are using cookies to implement functions like login, shopping cart or language selection for this website. Furthermore we use Google Analytics to create anonymized statistical reports of the usage which creates Cookies too. You will find more information in our privacy policy.
OK, I agree I do not want Google Analytics-Cookies
Quintessence International



Forgotten password?


Quintessence Int 43 (2012), No. 3     30. Jan. 2012
Quintessence Int 43 (2012), No. 3  (30.01.2012)

Online Article, Page 263, PubMed:22299127

Online Article: Oral and systemic manifestations of mucopolysaccharidosis type VI: A report of seven cases
Almeida-Barros, Renata Quirino de / Oka, Salomão Cury-Rad / Pordeus, Ana Carolina Barbosa / Medeiros, Paula Frassinetti Vasconcelos de / Bento, Patricia Meira / Godoy, Gustavo Pina
Mucopolysaccharidosis (MPS) is a group of rare metabolic diseases characterized by intralysosomal accumulation of glycosaminoglycans. MPS type VI or Maroteaux-Lamy syndrome is an autosomal-recessive syndrome caused by mutations in the lysosomal enzyme arylsulfatase B. A defect in the gene leads to accumulation of nondegraded mucopolysaccharides, resulting in severe cellular dysfunction with multisystem expression. The oral manifestations of MPS VI are not well described in the literature. This paper presents a series of seven patients with MPS VI, with the description of the general clinical manifestations and focus on the still rarely studied oral manifestations of the syndrome. Among them were high palate, open bite, impacted and/or included teeth, thickening of the pericoronal follicle, and changes in the temporomandibular joint.

Keywords: arylsulfatase B, metabolic diseases, mucopolysaccharidosis, oral manfestations