REFERENCES

1. Pẽna DA, Nova AM, Pẽna JA, Ruiz SH. Cleft foot and ectrodactyly-ectodermic dysplasia-cleft lip/palate syndrome Review of the literature and report of two new cases. Foot 2004;14:221-6.

2. South AP, Ashton GH, Willoughby C, Ellis IH, Bleck O, Hamada T, Mannion G, Wessagowit V, Hashimoto T, Eady RA, McGrath JA. EEC (Ectrodactyly, 3. 3. Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis. Br J Dermatol 2002;146:216-20.

3. Robinson GC, Wildervanek LS, Chiang TP. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome. Its association with conductive hearing loss. J Pediatr 1973;82:107-9.

4. Rüdiger RA, Haase W, Passarge E. Association of ectrodactyly, ectodermal dysplasia, and cleft lip-palate. Am J Dis Child 1970;120:160-3.

5. Marwaha M, Nanda KD. Ectrodactyly, ectodermal dysplasia, cleft lip, and palate (EEC syndrome). Contemp Clin Dent 2012;3:205-20.

6. Oğur G, Yüksel M. Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey. J Med Genet 1988;25:37-40.

7. Brunner HG, Hamel BC, Van Bokhoven H. The p63 gene in EEC and other syndromes. J Med Genet 2002;39:377-81.

8. Balci S, Engiz O, Okten G, Sipahier M, Gursu G, Kandemir B. A 19-year follow-up of a patient with type 3 ectrodactyly-ectodermal dysplasia-clefting syndrome who developed non-Hodgkin lymphoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2009;108:e91-5.

9. Soekarman D, Fryns JP. Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity? J Med Genet 1992;30:245-7.

10. Rosenberg JB, Butrus S, Bazemore MG. Ectrodactyly-ectodermal dysplasia-clefting syndrome causing blindness in a child. JAAPOS 2011;15:80-2.

11. Celli J, Duijf P, Hamel BC, Bamshad M, Kramer B, Smits Ap, Newbury-Ecob R, Hennekam RC, van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H. Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome. Cell 1999;99:143-53.

12. Levrero M, De Laurenzi V, Costanzo A, Gong J, Wang JY, Melino G. The p53/p63/p73 family of transcription factors: overlapping and distinct functions. J Cell Sci 2000;113:1661-70.

13. Yang A, Schweitzer R, Sun D, Kaghad M, Walker N, Bronson RT, Tabin C, Sharpe A, Caput D, Crum C, McKeon F. p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 1999;398:714-8.

14. Agrawal A, Agrawal R, Singh R, Agrawal R, Agrawal S. Lobster claw deformity. Indian J Dent Res 2014;25:243-7.

15. Blauth W, Borisch NC. Cleft feet. Proposals for a new classification based on roentgenographic morphology. Clin Orthop Relat Res 1990;258:41-8.

16. Freire-Maia N, Pinheiro M. Ectodermal dysplasias: a clinical and genetic study. New York: Alan R Liss; 1984. pp. 172-3.

17. Freire-Maia N. Ectodermal dysplasias. Hum Hered 1971;21:309-12.

18. Fosko SW, Stenn KS, Bolognia JL. Ectodermal dysplasias associated with clefting: significance of scalp dermatitis. J Am Acad Dermatol 1992;27:249-56.

19. Thakkar S, Marfatia Y. EEC syndrome sans clefting: Variable clinical presentations in a family. Indian J Dermatol Venereol Leprol 2007;73:46-8.

20. Dipak NK, Sheikh S, Srinivasan A. EEC (Ectrodactyly-Ectodermal dysplasia Clefting) Syndrome in a Newly Born Baby. Int J Intg Med Sci 2015;2:87-9.

21. Rodini ES, Richieri-Costa A. EEC Syndrome: report on 20 new patients, clinical and genetic considerations. Am J Med Genet 1990;37:42-53.

22. Koul M, Dwivedi R, Upadhyay V. Ectrodactyly-ectodermal dysplasia clefting syndrome (EEC syndrome). J Oral Biol Craniofac Res 2014;4:135-9.

23. Dhar RS, Bora A. Ectrodactyly-ectodermal dysplasia-cleft lip and palate syndrome. J Indian Soc Pedod Prev Dent 2014;32:346-9.

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