Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; relation to medical conditions?

References

• Robin NH, Shprintzen RJ. Defining the clinical spectrum of deletion 22q11.2. J Pediatr 2005;147:90–6.
   PubMedGoogle Scholar
• Shprintzen RJ. Velo-cardio-facial syndrome: 30 years of study. Dev Disabil Res Rev 2008;14:3–10.
   PubMed Web of Science ®Google Scholar
• Oskarsdóttir S, Vujic M, Fasth A. Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden. Arch Dis Child 2004;89:148–51.
   PubMed Web of Science ®Google Scholar
• Yamagishi H. The 22q11.2 deletion syndrome. Keio J Med 2002;51:77–88.
   PubMedGoogle Scholar
• Yamagishi H, Srivastava D. Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome. Trends Mol Med 2003;9:383–9.
   PubMed Web of Science ®Google Scholar
• Børglum Jensen S, Jacobsen P, Rotne L, Enk C, Illum F. Oral findings in DiGeorge syndrome. Int J Oral Surg 1983;12:250–4.
   PubMedGoogle Scholar
• Fukui N, Amano A, Akiyama S, Daikoku H, Wakisaka S, Morisaki I. Oral findings in Digeorge syndrome: clinical features and histologic study of primary teeth. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2000;89:208–15.
   PubMed Web of Science ®Google Scholar
• Klingberg G, Oskarsdóttir S, Johannesson EL, Norén JG. Oral manifestations in 22q11 deletion syndrome. Int J Paediatr Dent 2002;12:14–23.
   PubMedGoogle Scholar
• Klingberg G, Dietz W, Oskarsdóttir S, Odelius H, Gelander L, Norén JG. Morphological appearance and chemical composition of enamel in primary teeth from patients with 22q11 deletion syndrome. Eur J Oral Sci 2005;113:303–11.
   PubMedGoogle Scholar
• Mitsiadis TA, Tucker AS, De Bari C, Cobourne MT, Rice DP. A regulatory relationship between Tbx1 and FGF signaling during tooth morphogenesis and ameloblast lineage determination. Dev Biol 2008;320:39–48.
   PubMedGoogle Scholar
• Catón J, Luder HU, Zoupa M, Bradman M, Bluteau G, Tucker AS, Enamel-free teeth: Tbx1 deletion affects amelogenesis in rodent incisors. Dev Biol 2009;328:493–505.
   PubMedGoogle Scholar
• Lima K, Abrahamsen TG, Wolff AB, Husebye E, Alimohammadi M, Kämpe O Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome. Eur J Endocrinol 2011;165:345–52.
   PubMedGoogle Scholar
• Skjaerven R, Gjessing HK, Bakketeig LS. Birthweight by gestational age in Norway. Acta Obstet Gynecol Scand 2000;79:440–9.
   PubMed Web of Science ®Google Scholar
• da Silva Dalben G, Richieri-Costa A, de Assis Taveira LA. Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2008;106:e46–51.
   PubMedGoogle Scholar
• Nordgarden H, Jensen JL, Storhaug K. Reported prevalence of congenitally missing teeth in two Norwegian counties. Community Dent Health 2002;19:258–61.
   PubMedGoogle Scholar
• Suckling GW, Pearce EI. Developmental defects of enamel in a group of New Zealand children: their prevalence and some associated etiological factors. Commun Dent Oral Epidemol 1984;12:177–84.
   PubMed Web of Science ®Google Scholar
• Jälevik B, Klingberg G, Barregård L, Norén JG. The prevalence of demarcated opacities in permanent first molars in a group of Swedish children. Acta Odontol Scand 2001;59:255–60.
   PubMed Web of Science ®Google Scholar
• Jälevik B. Prevalence and diagnosis of molar-incisor-hypomineralisation (MIH): a systematic review. Eur Arch Paediatr Dent 2010;11:59–64.
   PubMedGoogle Scholar
• Hallett KB, Radford DJ, Seow WK. Oral health of children with congenital cardiac diseases: a controlled study. Pediatr Dent 1992;14:224–30.
   PubMedGoogle Scholar
• Tasioula V, Balmer R, Parsons J. Dental health and treatment in a group of children with congenital heart disease. Pediatr Dent 2008;30:323–8.
   PubMed Web of Science ®Google Scholar
• Moynihan PJ. The role of diet and nutrition in the etiology and prevention of oral diseases. Bull World Health Organ 2005;83:694–9.
   PubMed Web of Science ®Google Scholar
• Jensen SB, Illum F, Dupont E. Nature and frequency of dental changes in idiopathic hypoparathyroidism and pseudohypoparathyroidism. Scand J Dent Res 1981;89:26–37.
   PubMedGoogle Scholar
• Noren JG, Alm J. Congenital hypothyroidism and changes in the enamel of deciduous teeth. Acta Paediatr Scand 1983;72:485–9.
   PubMedGoogle Scholar
• Perheentupa J. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. J Clin Endocrinol Metab 2006;91:2843–50.
   PubMed Web of Science ®Google Scholar
• Pavlic A, Waltimo-Sirén J. Clinical and microstructural aberrations of enamel of deciduous and permanent teeth in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. Arch Oral Biol 2009;54:658–65.
   PubMedGoogle Scholar
• Jerome LA, Papaioannou VE. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1. Nat Genet 2001;27:286–91.
   PubMed Web of Science ®Google Scholar
• Klingberg G, Lingström P, Oskarsdóttir S, Friman V, Bohman E, Carlén A. Caries-related saliva properties in individuals with 22q11 deletion syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007;103:497–504.
   PubMed Web of Science ®Google Scholar