Diversity of clinical, radiographic and genealogical findings in 41 families with amelogenesis imperfecta

被引:14
作者
Adorno-Farias, Daniela [1 ,7 ]
Ortega-Pinto, Ana [1 ,7 ]
Gajardo, Paulina [2 ]
Salazar, Ana [3 ]
Morales-Bozo, Irene [4 ]
Werlinger, Fabiola [4 ]
Rojas-Flores, Sandra [5 ]
Molina-Berrios, Alfredo [4 ,7 ]
Echeverria-Lopez, Sonia [5 ]
Jara-Sandoval, Jose [4 ,7 ]
Jara, Lilian [6 ,7 ]
Urzua, Blanca [4 ,7 ]
机构
[1] Univ Chile, Fac Odontol, Dept Patol & Med Oral, Santiago, Chile
[2] Univ Chile, Fac Odontol, Santiago, Chile
[3] Univ Chile, Fac Odontol, Programa Magister Ciencias Odontol, Santiago, Chile
[4] Univ Chile, Fac Odontol, Inst Invest Ciencias Odontol, Ave Sergio Livingstone 943, Santiago, Chile
[5] Univ Chile, Fac Odontol, Dept Nino & Ortopedia Dentomaxilar, Santiago, Chile
[6] Univ Chile, Fac Med, Inst Ciencias Biomed, Santiago, Chile
[7] U Odontol Red Invest Enfermedades Orales Compleja, Santiago, Chile
关键词
Amelogenesis Imperfecta; Dental enamel; Malformations; Hypoplasia; Hypomineralization; DIAGNOSIS; MUTATION; ENAMEL;
D O I
10.1590/1678-7757-2018-0359
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Amelogenesis imperfecta (AI) is a group of enamel development disorders that alter the structure and chemical composition of the tissue. There is great variability in the clinical presentation; according to Witkop, AI can be categorized into 14 subtypes, which makes its diagnosis extremely complex. Objective: This study aimed to describe and determine the frequency of clinical and radiographic features and inheritance patterns found in 41 Chilean families diagnosed with diverse types of AI. Material and Methods: We analyzed the clinical records, photographs, pedigrees and radiographs of 121 individuals recruited between 2003 and 2016. All of the information was included in a database that was analyzed using the application Stata 14. Results: The 72 affected individuals had average age of 16 years, and no sex association with the presence of AI was found. The most frequent clinical subtypes were as follows: 43% hypomature, 25% hypoplastic, 21% hypomature/hypoplastic, 7% hypocalcified and 4% hypocalcified/hypoplastic. The number of severely affected teeth was 22, which occurred in the patients with hypocalcified and hypocalcified/hypoplasic AI who presented the highest number of damaged teeth. Caries and periodontal disease were found in 47 and 32% of the patients, respectively. Malocclusions were observed in 43% of the individuals with AI, with open bite being the most frequent. Radiographically, the thickness of the enamel decreased in 51% of the patients, and 80% showed decreased radiopacity of the enamel compared to that of dentin. Autosomal dominant inheritance pattern was found in 37% of the families with hypoplastic AI, and autosomal recessive pattern was present in 56% of the other clinical subtypes, but more frequently in those affected with hypomature and hypocalcified AI. Conclusion: Of the five clinical subtypes, autosomal recessive hypomature, autosomal dominant hypoplastic and autosomal recessive hypomature/hypoplastic AI were the most prevalent subtypes in this group.
引用
收藏
页数:11
相关论文
共 30 条
  • [1] Alachioti Xanthippi Sofia, 2014, J Orthod Sci, V3, P1, DOI 10.4103/2278-0203.127547
  • [2] Amelogenesis imperfecta: a classification and catalogue for the 21st century
    Aldred, MJ
    Savarirayan, R
    Crawford, PJM
    [J]. ORAL DISEASES, 2003, 9 (01) : 19 - 23
  • [3] BACKMAN B, 1988, SCAND J DENT RES, V96, P505
  • [4] Cartwright AR, 1999, J CRAN GENET DEV BIO, V19, P148
  • [5] Chaitanya V, 2014, Indian J Nephrol, V24, P260, DOI 10.4103/0971-4065.133043
  • [6] Target gene analyses of 39 amelogenesis imperfecta kindreds
    Chan, Hui-Chen
    Estrella, Ninna M. R. P.
    Milkovich, Rachel N.
    Kim, Jung-Wook
    Simmer, James P.
    Hu, Jan C-C.
    [J]. EUROPEAN JOURNAL OF ORAL SCIENCES, 2011, 119 : 311 - 323
  • [7] Amelogenesis imperfecta
    Crawford, Peter J. M.
    Aldred, Michael
    Bloch-Zupan, Agnes
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2007, 2 (1)
  • [8] Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations
    de la Dure-Molla, Muriel
    Quentric, Mickael
    Yamaguti, Paulo Marcio
    Acevedo, Ana-Carolina
    Mighell, Alan J.
    Vikkula, Miikka
    Huckert, Mathilde
    Berdal, Ariane
    Bloch-Zupan, Agnes
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2014, 9
  • [9] Encinas RP, 2001, QUINTESSENCE INT, V32, P183
  • [10] Amelogenesis imperfecta: an introduction
    Gadhia, K.
    McDonald, S.
    Arkutu, N.
    Malik, K.
    [J]. BRITISH DENTAL JOURNAL, 2012, 212 (08) : 377 - 379