Abstract

Case Report

The Pierre Marie-Sainton syndrome: Report of a family

Salem Y*, Omar Y, Dorsaf S, Sonia M, Samir B and Olfa B

Published: 28 August, 2019 | Volume 4 - Issue 2 | Pages: 012-014

Pierre Maria and Sainton syndrome or cleido-cranial dysplasia (CCD) is a rare syndrome presenting an autosomal pattern of inheritance, characterized by characterized by a triad: clavicular aplasia, delayed ossification of the fontanelles and sutures of the vault of the skull. To these may be added multiple dental inclusions.

Read Full Article HTML DOI: 10.29328/journal.johcs.1001028 Cite this Article Read Full Article PDF

References

  1. Lu Y, Li Y, Cavender AC, Wang S, Mansukhani A, et al. Molecular studies on the roles of Runx2 and Twist1 in regulating FGF signaling. Dev Dyn. 2012; 241: 1708-1715. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22972545
  2. Marie P, Sainton P. Sur la dysostose cleido-crânienne héréditaire. Rev neurol. 1898; 6: 835-838.
  3. Kallialia E, Taskinen PJ. Cleidocranial dysostosis: report of six typical cases and one atypical case. Oral Surg Oral Med Oral Pathol. 1962; 14: 808. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/14453327
  4. De Nguyen T, Turcotte JY. Cleidocranial dysplasia: review of literature and presentation of a case. J Can Dent Assoc. 1994; 60:1073-1078. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/7842373
  5. Golan I, Baumert U, Hrala BP, Müβig D. Dentomaxillofacial variability of cleidocranial dysplasia: Clinicoradiological presentation and systemic review. Dentomaxillofac Radiol. 2003; 32:347-54. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/15070835
  6. Garg RK, Argawal P. Clinical spectrum of cleidocranial dysplasia: a case report. Cases J. 2008; 1: 377-381. PubMed: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614945/
  7. Nehta DN, Vachhani RV, Patel MB. Cleidocranial dysplasia: a report of two cases. J Indian Soc Pedod Prev Pent 2011 ; 29 : 251-254. PubMed: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869578/
  8. Thamzih Chelvan H, Malathi N, Vignesh Kailasam, Ponnidurai A. Cleidocranial dysplasia: a family report. Journal of Indian society of pedodontics and preventive dentistry. 2009; 4: 249-252. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/19915277
  9. Brueton LA, Reeve A, Ellis R, Husband P, Thompson EM, et al. Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three indiciduals. Am J Med Genet. 1992; 43: 612-618. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/1605259
  10. Prakash R, Mohan S, Suma GN, Vashishth S, Goel S. Cleidocranial dysplasia: clinic-radiological illustration of a rare case. J oral science 2010; 1: 161-166. PubMed: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129351/
  11. Cooper SC, Flaitz CM, Johnston DA, Lee B, Hecht JT. A natural history of cleidocranial dysplasia. Am J Med Genet. 2001; 104: 1-6. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11746020
  12. Mc Namara CM, O’Riordan BC, Blake M, Sandy JR. Cleidocranial dysplasia: radiological appearances on dental panoramic radiography. Dentomaxillofac Radiol. 1999; 28: 89-97. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/10522197
  13. Tanaka JL, Ono Filho MH, Castilho JC, Moraes LC. Cleidocranial dysplasia: importance of radiographic imagines in diagnosis of this condition. J Oral Sci. 2006; 48: 161-166. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/17023750
  14. Gonzalez Lopez BS, Ortiz Solalinde, Kubodera Itro T, Lara Carillo E, Ortiz Solalinde E. Cleidocranial dysplasia: report of a family. J Oral Sci. 2004; 46: 259-266.
  15. Roberts T, Stephen L, Beighton P. Cleidocranial dysplasia: a review of the dental, historical, and practical implications with an overview of the South African experience. Oral Med. 2013; 115: 45-55. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/23102800

Figures:

Figure 1

Figure 1

Figure 1

Figure 2

Figure 1

Figure 3

Similar Articles

Recently Viewed

Read More

Most Viewed

Read More

Help ?