La dysplasie cléidocrânienne : trois cas familiaux

Auteur/ices

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

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Références

Garg RK, Argawal P. Clinical spectrum of cleidocranial dysplasia: a case report. Agrawal. Cases J 2008; 1:377-81.

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.

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.

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.

Wang GX, Sun RP, Song FL. A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia. Genet Mol Res 2010;9:41-7.

Kallialia E, Taskinen PJ. Cleidocranial dysostosis: report of six typical cases and one atypical case. Oral Surg Oral Med Oral Pathol 1962;14:808.

Nehta DN, Vachhani RV, Patel MB. Cleidocranial dysplasia: a report of two cases. J Indian Soc Pedod Prev Pent 2011; 29 : 251-4.

Thamzih Chelvan H, Malathi N, Vignesh Kailasam, Ponnidurai A. Cleidocranial dysplasia: a family report. J Indian Soc Pedod Prev Pent 2009; 4:249-52.

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Publiée

2015-12-02

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