2019, Number 2
<< Back Next >>
Rev Odont Mex 2019; 23 (2)
Amelogenesis imperfecta in pediatric patients: a case series
Simancas EV, Natera A, Acosta CMG
Language: Spanish
References: 25
Page: 97-106
PDF size: 314.48 Kb.
ABSTRACT
The Amelogenesis imperfecta (AI) is a genetic abnormality that affects the structure of tooth enamel and can lead to problems with sensitivity, dental esthetics, and function, as well as psychological alterations in self-esteem and self-image. The study of the AI genetic regulation allows for a better understanding of its pathogenesis. This research aimed to describe the oral clinical characteristics of pediatric patients with AI. A case series was formed from a non-randomized convenience sample of 6 children aged 8 to 13 years who attended the private practice for concern about dental esthetics. The most prevalent AI was the hypoplastic type. AI is a quantitative or qualitative enamel disorder that produces changes in tooth color and texture; it affects mostly all teeth and shows a genetic pattern.
REFERENCES
Lacruz RS, Nanci A, Kurtz I, Wright JT, Paine ML. Regulation of pH during amelogenesis. Calcif Tissue Int. 2010; 86 (2): 91-103. doi: 10.1007/s00223-009-9326-7.
Zheng L, Ehardt L, McAlpin B, About I, Kim D, Papagerakis S et al. The tick tock of odontogenesis. Experimental Cell Research. 2014; 325 (2): 83-89. doi: 10.1016/j.yexcr.2014.02.007.
Acosta de Camargo MG. Defectos de esmalte en la población infantil. Revisión bibliográfica. ODOUS científica. 2010; 11 (1): 51-58.
Hubbard MJ, Mangum JE, Perez VA, Nervo GJ, Hall RK. Molar hypomineralisation: a call to arms for enamel researchers. Front Physiol. 2017; 8: 546.
Prasad MK, Laouina S, El Alloussi M, Dollfus H, Bloch-Zupan A. Amelogenesis imperfecta: 1 family, 2 phenotypes, and 2 mutated genes. J Dent Res. 2016; 95 (13): 1457-1463. doi: 10.3389/fphys.2017.00546.
Seedorf H, Klaften M, Eke F, Fuchs H, Seedorf U, Hrabe de Angelis M. A mutation in the enamelin gene in a mouse model. J Dent Res. 2007; 86 (8): 764-768. doi: 10.1177/154405910708600815.
Smith CEL, Poulter JA, Antanaviciute A, Kirkham J, Brookes SJ, Inglehearn CF et al. Amelogenesis imperfecta; genes, proteins, and pathways. Front Physiol. 2017; 8: 435. doi: 10.3389/fphys.2017.00435.
Crawford PJM, Aldred M, Bloch-Zupan A. Amelogenesis imperfecta. Orphanet J Rare Dis. 2007; 2: 17. doi: 10.1186/1750-1172-2-17.
Chamarthi V, Varma BR, Jayanthi M. Amelogenesis imperfecta: a clinician’s challenge. J Indian Soc Pedod Prev Dent. 2012; 30 (1): 70-73. doi: 10.4103/0970-4388.95587.
Witkop CJ. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol. 1988; 17 (9-10): 547–553. doi: 10.1111/j.1600-0714.1988.tb01332.x
Oliveira AFB, Chaves AMB, Rosenblatt A. The influence of enamel defects on the development of early childhood caries in a population with low socioeconomic status: a longitudinal study. Caries Res. 2006; 40 (4): 296-302. doi: 10.1159/000093188.
Uribe S. Early childhood caries--risk factors. Evid Based Dent. 2009; 10 (2): 37-38. doi: 10.1038/sj.ebd.6400642.
Simancas-Escorcia V, Berdal A, Díaz-Caballero A. Caracterización fenotípica del síndrome amelogénesis imperfecta–nefrocalcinosis: una revisión. Duazary. 2019; 16 (1): 129-143. doi: 10.21676/2389783X.2531.
Aren G, Ozdemir D, Firatli S, Uygur C, Sepet E, Firatli E. Evaluation of oral and systemic manifestations in an amelogenesis imperfecta population. J Dent. 2003; 31 (8): 585-591. doi: 10.1016/s0300-5712(03)00116-7.
Hoppenreijs TJ, Voorsmit RA, Freihofer HP, van’t Hof MA. Open bite deformity in amelogenesis imperfecta. Part 2: Le Fort I osteotomies and treatment results. J Craniomaxillofac Surg. 1998; 26 (5): 286-293. doi: 10.1016/s1010-5182(98)80056-5.
Acevedo AC, Poulter JA, Alves PG, de Lima CL, Castro LC, Yamaguti PM et al. Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations. BMC Med Genet. 2015; 16: 8. doi: 10.1186/s12881-015-0154-5.
Lindemeyer RG, Gibson CW, Wright TJ. Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations. Pediatr Dent. 2010; 32 (1): 56-60.
Coffield KD, Phillips C, Brady M, Roberts MW, Strauss RP, Wright JT. The psychosocial impact of developmental dental defects in people with hereditary amelogenesis imperfecta. J Am Dent Assoc. 2005; 136 (5): 620-630. doi: 10.14219/jada.archive.2005.0233.
Montero-Martín J, Bravo-Pérez M, Albaladejo-Martínez A, Hernández-Martín LA, Rosel-Gallardo EM. Validation the Oral Health Impact Profile (OHIP-14sp) for adults in Spain. Med Oral Patol Oral Cir Bucal. 2009; 14 (1): E44-E50.
Stokes E, Ashcroft A, Platt MJ. Determining Liverpool adolescents’ beliefs and attitudes in relation to oral health. Health Educ Res. 2006; 21 (2): 192-205. doi: 10.1093/her/cyh055.
Calero JA, Soto L. Amelogénesis imperfecta. Informe de tres casos en una familia en Cali, Colombia. Colombia Médica. 2005; 36 (4 Supl 3): 47-50.
Sholapurkar AA, Joseph RM, Varghese JM, Neelagiri K, Acharya SRR, Hegde V et al. Clinical diagnosis and oral rehabilitation of a patient with amelogenesis imperfecta: a case report. J Contemp Dent Pract. 2008; 9 (4): 92-98.
Elizabeth J, Lakshmi-Priya E, Umadevi KMR, Ranganathan K. Amelogenesis imperfecta with renal disease--a report of two cases. J Oral Pathol Med. 2007; 36 (10): 625-628. doi: 10.1111/j.1600-0714.2007.00615.x
Mete JJ, Dange SP, Khalikar AN, Vaidya SP. Functional and esthetic rehabilitation of mutilated dentition associated with amelogenesis imperfecta. J Indian Prosthodont Soc. 2012; 12 (2): 94-100. doi: 10.1007/s13191-011-0102-9.
Varela-Morales M, Botella-Pérez JM, Jiménez-Garcia J, García-Camba Varela P. Interdisciplinary treatment of a patient with amelogenesis imperfecta. J Clin Orthod. 2010; 44 (9): 553-559.