Research Article
The Pierre Marie-Sainton syndrome: Report of a family
Salem Y*, Omar Y, Dorsaf S, Sonia M, Samir B and Olfa B
Published: 08/28/2019 | Volume 4 - Issue 2 | Pages: 012-014
Abstract
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
References
- 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
- Marie P, Sainton P. Sur la dysostose cleido-crânienne héréditaire. Rev neurol. 1898; 6: 835-838.
- 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
- 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
- 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
- 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/
- 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/
- 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
- 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
- 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/
- 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
- 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
- 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
- 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.
- 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