Accès gratuit
Numéro |
Med Sci (Paris)
Volume 40, Numéro 1, Janvier 2024
La cavité orale et les dents au cœur de la santé
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Page(s) | 16 - 23 | |
Section | M/S Revues | |
DOI | ||
Publié en ligne | 1 février 2024 |
- Yuan Y, Chai Y. Regulatory mechanisms of jaw bone and tooth development. Curr Top Dev Biol 2019; 133 : 91–118.
- Babajko S, Gayrard V, Houari S, et al. La sphère orale, cible et marqueur de l’exposition environnementale. I. Défauts du développement dentaire. Med Sci (Paris) 2020; 36 : 225–30. [EDP Sciences]
- Collignon A-M, Vergnes J-N, Germa A, et al. Factors and Mechanisms Involved in Acquired Developmental Defects of Enamel : A Scoping Review. Front Pediatr 2022; 10 : 836708.
- de La Dure-Molla M, Fournier BP, Manzanares MC, et al. Elements of morphology : Standard terminology for the teeth and classifying genetic dental disorders. Am J Med Genet A 2019; 179 : 1913–81.
- de la Dure-Molla M, Quentric M, Yamaguti PM, et al. Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. Orphanet J Rare Dis 2014; 9 : 84.
- Linglart A, Biosse-Duplan M. Hypophosphatasia. Curr Osteoporos Rep 2016; 14 : 95–105.
- Bloch-Zupan A, Vaysse F. Hypophosphatasia : oral cavity and dental disorders. Arch Pediatr 2017; 24 : 5S80–85S84.
- Yu T, Klein OD. Molecular and cellular mechanisms of tooth development, homeostasis and repair. Development 2020; 147 : dev184754.
- Balic A. Concise Review : Cellular and Molecular Mechanisms Regulation of Tooth Initiation. Stem Cells 2019; 37 : 26–32.
- Bloch-Zupan A, Jamet X, Etard C, et al. Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects. Am J Hum Genet 2011; 89 : 773–81.
- Nassif A, Lignon G, Asselin A, et al. Transcriptional Regulation of Jaw Osteoblasts : Development to Pathology. J Dent Res 2022; 101 : 859–69.
- Zhang H, Gong X, Xu X, et al. Tooth number abnormality : from bench to bedside. Int J Oral Sci 2023; 15 : 5.
- Wright JT, Abbott BM, Salois MN, et al. Rare diseases of ectoderm : Translating discovery to therapy. Am J Med Genet A 2023; 191 : 902–9.
- Smith CEL, Poulter JA, Antanaviciute A, et al. Amelogenesis Imperfecta; Genes, Proteins, and Pathways. Front Physiol 2017; 8 : 435.
- Talaat DM, Hachim IY, Afifi MM, et al. Assessment of risk factors and molecular biomarkers in children with supernumerary teeth : a single-center study. BMC Oral Health 2022; 22 : 117.
- Arte S, Parmanen S, Pirinen S, et al. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations. PLoS One 2013; 8 : e73705.
- Chu K-Y, Wang Y-L, Chou Y-R, et al. Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis. J Pers Med 2021; 11 : 1217.
- Yu M, Wong S-W, Han D, et al. Genetic analysis : Wnt and other pathways in nonsyndromic tooth agenesis. Oral Dis 2019; 25 : 646–51.
- Fournier BP, Bruneau MH, Toupenay S, et al. Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated Genes. J Dent Res 2018; 97 : 1306–16.
- Bowles B, Ferrer A, Nishimura CJ, et al. TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss : A novel cohort study. Am J Med Genet A 2021; 185 : 2417–33.
- Kunz F, Kayserili H, Midro A, et al. Characteristic dental pattern with hypodontia and short roots in Fraser syndrome. Am J Med Genet A 2020; 182 : 1681–9.
- Prasad MK, Geoffroy V, Vicaire S, et al. A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement. J Med Genet 2016; 53 : 98–110.
- Tardieu C, Jung S, Niederreither K, et al. Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations : A multicentric genotype-phenotype study. Clin Genet 2017; 92 : 477–86.
- Lignon G, de la Dure-Molla M, Dessombz A, et al. L’émail - Un autoassemblage unique dans le monde du minéral. Med Sci (Paris) 2015; 31 : 515–521. [EDP Sciences]
- Bloch-Zupan A, Rey T, Jimenez-Armijo A, et al. Amelogenesis imperfecta : Next-generation sequencing sheds light on Witkop’s classification. Front Physiol 2023; 14 : 1130175.
- Lacruz RS, Habelitz S, Wright JT, et al. Dental enamel formation and implications for oral health and disease. Physiol Rev 2017; 97 : 939–93.
- Bardet C, Courson F, Wu Y, et al. Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation. J Bone Miner Res 2016; 31 : 498–513.
- Yamaguti PM, Neves F de AR, Hotton D, et al. Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. J Med Genet 2017; 54 : 26–37.
- Simancas Escorcia V, Diarra A, Naveau A, et al. Lack of FAM20A, Ectopic Gingival Mineralization and Chondro/Osteogenic Modifications in Enamel Renal Syndrome. Front Cell Dev Biol 2020; 8 : 605084.
- Dubail J, Huber C, Chantepie S, et al. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. Nat Commun 2018; 9 : 3087.
- Simmer JP, Richardson AS, Wang S-K, et al. Ameloblast transcriptome changes from secretory to maturation stages. Connect Tissue Res 2014; 55 : 29–32.
- Sharir A, Marangoni P, Zilionis R, et al. A large pool of actively cycling progenitors orchestrates self-renewal and injury repair of an ectodermal appendage. Nat Cell Biol 2019; 21 : 1102–12.
- Krivanek J, Soldatov RA, Kastriti ME, et al. Dental cell type atlas reveals stem and differentiated cell types in mouse and human teeth. Nat Commun 2020; 11 : 4816.
- Fresia R, Marangoni P, Burstyn-Cohen T, et al. From Bite to Byte : Dental Structures Resolved at a Single-Cell Resolution. J Dent Res 2021; 100 : 897–905.
- Opsahl Vital S, Gaucher C, Bardet C, et al. Tooth dentin defects reflect genetic disorders affecting bone mineralization. Bone 2012; 50 : 989–97.
- Kovacs CS, Chaussain C, Osdoby P, et al. The role of biomineralization in disorders of skeletal development and tooth formation. Nat Rev Endocrinol 2021; 17 : 336–49.
- Mortier GR, Cohn DH, Cormier-Daire V, et al. Nosology and classification of genetic skeletal disorders : 2019 revision. Am J Med Genet A 2019; 179 : 2393–419.
- de La Dure-Molla M, Philippe Fournier B, Berdal A. Isolated dentinogenesis imperfecta and dentin dysplasia : revision of the classification. Eur J Hum Genet 2015; 23 : 445–51.
- Yamaguti PM, de La Dure-Molla M, Monnot S, et al. Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta. J Dent Res 2023; 102 : 616–25.
- Thumbigere-Math V, Alqadi A, Chalmers NI, et al. Hypercementosis Associated with ENPP1 Mutations and GACI. J Dent Res 2018; 97 : 432–41.
- Beck-Nielsen SS, Mughal Z, Haffner D, et al. FGF23 and its role in X-linked hypophosphatemia-related morbidity. Orphanet J Rare Dis 2019; 14 : 58.
- Bacchetta J, Bardet C, Prié D. Physiology of FGF23 and overview of genetic diseases associated with renal phosphate wasting. Metabolism 2020; 103S : 153865.
- McKee MD, Hoac B, Addison WN, et al. Extracellular matrix mineralization in periodontal tissues : Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemia. Periodontol 2000 2013; 63 : 102–22.
- Chaussain-Miller C, Sinding C, Wolikow M, et al. Dental abnormalities in patients with familial hypophosphatemic vitamin D-resistant rickets : prevention by early treatment with 1-hydroxyvitamin D. J Pediatr 2003; 142 : 324–31.
- Biosse Duplan M, Coyac BR, Bardet C, et al. Phosphate and Vitamin D Prevent Periodontitis in X-Linked Hypophosphatemia. J Dent Res 2017; 96 : 388–95.
- Boukpessi T, Hoac B, Coyac BR, et al. Osteopontin and the dento-os搜索引擎优化us pathobiology of X-linked hypophosphatemia. Bone 2017; 95 : 151–61.
- Ward LM, Glorieux FH, Whyte MP, et al. Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia. J Clin Endocrinol Metab 2022; 107 : e3241–53.
- Gadion M, Hervé A, Herrou J, et al. Burosumab and Dental Abscesses in Children With X-Linked Hypophosphatemia. JBMR Plus 2022; 6 : e10672.
- Le Norcy E, Reggio-Paquet C, de Kerdanet M, et al. Dental and craniofacial features associated with GNAS loss of function mutations. Eur J Orthod 2020; 42 : 525–33.
- Whyte JL, Smith AA, Helms JA. Wnt Signaling and Injury Repair. Cold Spring Harbor Perspectives in Biology 2012; 4 : a008078–a008078.
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