Literature DB >> 24919127

A clinical multicenter study of orofacial features in 26 brazilian patients with different types of mucopolysaccharidosis.

Erlane Marques Ribeiro, Cristiane S R Fonteles, Adriana Bezerra Freitas, Karla Shangela da Silva Alves, André Jalles Monteiro, Carlos Antônio Bruno da Silva.   

Abstract

PURPOSE: This study aimed to describe the orofacial features of 26 unrelated Brazilian patients with mucopolysaccharidosis and to verify any possible associations between these findings and specific types of mucopolysaccharidosis.
METHODS: Patients were diagnosed with mucopolysaccharidosis and clinically evaluated. Following consent, a clinical assessment form was completed. Facial and intraoral examination was performed by evaluating facial pattern, malocclusions, dental caries, and tooth identification.
RESULTS: Midface deficiency, increased lower facial third, anterior open bite, convex profile, macroglossia, gingival enlargement, and spaced arches were the most frequently observed features. These findings did not allow a differential diagnosis among the different types of mucopolysaccharidosis, except for pitting enamel, which significantly associated with mucopolysaccharidosis IVA (P < .001). Open bite was associated with mucopolysaccharidosis types I, II, III, and VI; however, only one patient with mucopolysaccharidosis IVA expressed this feature (P = .043).
CONCLUSIONS: Our results suggest that pitted enamel in patients with mucopolysaccharidosis is most likely a feature of mucopolysaccharidosis type IVA; whereas, open bite is rarely observed in these patients. Orofacial features in mucopolysaccharidosis may help pediatric dentists recognize this disorder and minimize the delay between the initial signs/symptoms and diagnosis of the disease. Future studies should focus on the longitudinal manifestations, expression, and severity of mucopolysaccharidosis-associated orofacial anomalies.

Entities:  

Keywords:  glycosaminoglycans; malocclusions; metabolic disorders; mucopolysaccharidosis; orofacial abnormalities

Mesh:

Year:  2014        PMID: 24919127     DOI: 10.1597/13-204

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  5 in total

1.  Differences in maxillomandibular morphology among patients with mucopolysaccharidoses I, II, III, IV and VI: a retrospective MRI study.

Authors:  Till Koehne; Anja Köhn; Reinhard E Friedrich; Uwe Kordes; Thorsten Schinke; Nicole Muschol; Bärbel Kahl-Nieke
Journal:  Clin Oral Investig       Date:  2017-10-18       Impact factor: 3.573

2.  Rare genetic diseases affecting skeletal development and oral health disparities among children and adolescents: a pathway analysis.

Authors:  Mario Vianna Vettore; Ana Cristina Borges-Oliveira; Heloisa Vieira Prado; Gabriela de Almeida Lamarca; Janine Owens
Journal:  Int Dent J       Date:  2020-07-17       Impact factor: 2.607

3.  The new frame for Mucopolysaccharidoses.

Authors:  Rossella Parini; Andrea Biondi
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

4.  Assessing a possible vulnerability to dental caries in individuals with rare genetic diseases that affect the skeletal development.

Authors:  Heloisa Vieira Prado; Natália Cristina Ruy Carneiro; Matheus França Perazzo; Mauro Henrique Nogueira Guimarães de Abreu; Carolina de Castro Martins; Ana Cristina Borges-Oliveira
Journal:  Orphanet J Rare Dis       Date:  2019-06-18       Impact factor: 4.123

5.  Pediatric Dental Management of an Uncommon Case of Mucopolysaccharidosis Type IV A (Morquio A Syndrome): A Case Report of a Three-Year Follow-Up.

Authors:  Andrea Gómez-González; Miguel Ángel Rosales-Berber; Paola De Ávila-Rojas; Amaury Pozos-Guillén; Arturo Garrocho-Rangel
Journal:  Case Rep Dent       Date:  2020-01-22
  5 in total

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