Oral and systemic manifestations of mucopolysaccharidosis type VI: A report of seven cases

Quintessence International

Volumn 43, Issue 3, 2012, Pages e32-e38

  De Almeida Barros, Renata Quirino ^a   Oka, Salomão Cury Rad ^a   Pordeus, Ana Carolina Barbosa ^b   De Medeiros, Paula Frassinetti Vasconcelos ^b   Bento, Patricia Meira ^a   Godoy, Gustavo Pina ^a  

^a STATE UNIVERSITY OF PARAÍBA   (Brazil)

^b FEDERAL UNIVERSITY OF CAMPINA GRANDE   (Brazil)

Author keywords

Arylsulfatase B; Metabolic diseases; Mucopolysaccharidosis; Oral manfestations

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CONGENITAL MALFORMATION; DIASTEMA; FEMALE; HUMAN; MACROGLOSSIA; MALE; MALOCCLUSION; MAROTEAUX LAMY SYNDROME; MOUTH DISEASE; PALATE; PATHOLOGY; PRESCHOOL CHILD; TEMPOROMANDIBULAR JOINT DISORDER; TOOTH DISEASE; TOOTH SAC;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DENTAL SAC; DIASTEMA; FEMALE; HUMANS; MACROGLOSSIA; MALE; MALOCCLUSION; MOUTH DISEASES; MUCOPOLYSACCHARIDOSIS VI; OPEN BITE; PALATE; TEMPOROMANDIBULAR JOINT DISORDERS; TOOTH, IMPACTED;

EID: 84864019139     PISSN: 00336572     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

1. Aumailley M, Gayraud B. Structure and biological activity of the extracelular matrix. J Mol Med (Berl) 1998; 76: 253-265.
2. Giugliani R, Harmatz P, Wraith JE. Manegement guidelines for mucopolysaccharidosis VI. Pediatrics 2007; 120: 405-418.
3. Azevedo AC, Schwartz IV, Kalakun L, et al. Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI. Clin Genet 2004; 66: 208-213.
4. Martins AM. Mucopolissacaridoses Manual de Orientações. São Paulo: Universidade Federal de São Paulo, 2002.
5. Alpöz AR, Coker M, Celen E, et al. The oral manifestations of Maroteaux-Lamy syndrome (mucopolysaccharidosis VI): A case report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006; 101: 632-637.
6. Martins AM, Gilvanetti D, Micheletti C, Silveira MT, D’Almeida V, Segal S. Prevalence of MPS VI patients in Brazil [abstract]. Mol Genet Metab 2009; 98: 86.
7. Krivit W. Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases. Springer Semin Immunopathol 2004; 26: 119-132.
8. Harmatz P, Giugliani R, Schwartz I, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double blind, placebo-controlled multinational study of recombinant human N-acetylgalactosamine-4-sulfatase B (rhASB) and follow-on, open-label extension study. J Pediatr 2006; 148: 533-539.
9. Brooks DA, Gibson GJ, Karageorgos L, Hein LK, Robertson EF, Hopwood JJ. An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum. Mol Genet Metab 2005; 85: 236-238.
10. Smith KS, Hallett KB, Hall RK, Wardrop RW, Firth N. Mucopolysaccharidosis: MPS VI and associated delayed tooth eruption. Int J Oral Maxillofac Surg 1995; 24: 176-180
11. Dangel J. Cardiovascular changes in children with mucopolysaccharide storage diseases and related disorders: Clinical and echocardiographic findings in 64 patients. Eur J Pediatr 1998; 157: 534-538.
12. Gomes BSD, Nóbrega CEB, Medeiros PFV, Medeiros IAMC, Pordeus ACB. Cardiac manifestations in patients with Mucopolysaccharidosis VI. Rev Bras Ecocardiogr Imagem Cardiovasc 2011; 24: 88-92.
13. Paula AC. Achados radiológicos em pacientes com mucopolissacaridosetipo VI (Síndrome de Maroteaux-Lamy). Rev Imagem 2006; 28: 7-12.
14. Gardner DG. The oral manifestations of Hurler’s syndrome. Oral Surg Oral Med Oral Pathol 1971; 32: 46-57.
15. Turra GS, Schwartz IVD. Evaluation of orofacial motricity in patients with mucopolysaccharidosis: A crosssectional study. J Pediatr (Rio J) 2009; 85: 254-260.
16. Horrigam WD, Baker DH. Gargoylism: A review of the roentgen skull changes with a description of a new finding. Am J Roentgenol Radium Ther Nucl Med 1961; 86: 473-477.
17. MacLeod SP, Macintyre DR. Bilateral hypoplasia of mandibular condyles in Hurler’s syndrome. Oral Surg Oral Med Oral Pathol 1993; 75: 659-660.
18. Roberts MW, Barton NW, Constantopoulos G, Butler DP, Donahue AH. Occurrence of multiple dentigerous cysts in a patient with the Maroteaux-Lamy syndrome (mucopolysaccharidosis, type VI). Oral Surg Oral Med Oral Pathol 1984; 58: 169-175.