Cleidocranial dysplasia: family cases

##plugins.themes.academic_pro.article.sidebar##

Published Dec 2, 2015
Download
pdf
Vol. 93 No. 7 (2015): Issue Jul 2015

##plugins.themes.academic_pro.article.main##

Olfa Bouyahia
Rania Ben Rebeh
Imene Bel Hadj
Samir Boukthir
Azza Sammoud

##plugins.themes.academic_pro.article.details##

References

  1. Garg RK, Argawal P. Clinical spectrum of cleidocranial dysplasia: a case report. Agrawal. Cases J 2008; 1:377-81.
  2. Prakash R, Mohan S, Suma GN, Vashishth S , Goel S. Cleidocranial dysplasia: clinicradiological ilustration of a rare case. J Oral Sci 2010;1:161-6.
  3. Wang S, Zhang S, Wang Y, Chen Y, Zhou L. Cleidocranial dysplasia syndrome: clinical characteristics and mutation study of a Chinese family. Int J Clin Exp Med 2013;6:900- 7.
  4. Brueton LA, Reeve A, Ellis R, Husband P, Thompson EM, Kingston HM. Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three indiciduals. Am J Med Genet 1992, 43:612-8.
  5. Wang GX, Sun RP, Song FL. A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia. Genet Mol Res 2010;9:41-7.
  6. Kallialia E, Taskinen PJ. Cleidocranial dysostosis: report of six typical cases and one atypical case. Oral Surg Oral Med Oral Pathol 1962;14:808.
  7. Nehta DN, Vachhani RV, Patel MB. Cleidocranial dysplasia: a report of two cases. J Indian Soc Pedod Prev Pent 2011; 29 : 251-4.
  8. Thamzih Chelvan H, Malathi N, Vignesh Kailasam, Ponnidurai A. Cleidocranial dysplasia: a family report. J Indian Soc Pedod Prev Pent 2009; 4:249-52.