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Salem K, Moazami F. Dental reconstruction in hypohydrotic ectodermal dysplasia: case report . ijpd 2016; 11 (2) :77-82
URL: http://jiapd.ir/article-1-121-en.html
Abstract:   (4496 Views)
Background and aim: Ectodermaldysplasia is a hereditary disorder of ectodermthat involvesteeth, skin, and hair, nails, salivary, lacrimal and sweat glands. The most common type of diseaseishypohydrotic ectodermal dysplasia that is inherited as recessive x-linked trait.
The main clinical symptoms are dry skin, sparse thinhair, small brittle nails, hyperkeratosis of palms and soles, complete or partial missing of sweat glands, hypodontia and oligodontia.
Case report:The patient was a six years oldfemalewith hypohydrotic ectodermal dysplasia with the chief complaint of difficult eating. The clinical and radiographic examinations showed conical teeth and microdontia, hypodontia, increased overbite, and atrophic alveolar ridge. The oral rehabilitation was performed by constructing overdentures on both jaws.The oral functions including mastication, speaking and esthetics were improved to a large extent.
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Case Report
 
 

Dental reconstruction in hypohydrotic ectodermal dysplasia: case report
Katayoun Salem1, Fatemeh Moazami2*
1.  Department of Pediatric Dentistry, School of Dentistry, Islamic Azad University, Tehran Branch, Tehran .Iran
2.  Postgraduate student, Dept. of Pediatric Dentistry, School of Dentistry, Islamic Azad University, Tehran Branch, Tehran .Iran
Corresponding author: Fatemeh Moazami
E mail: ft.moazami88@yahoo.ca  
 

Abstract
Background and aim: Ectodermaldysplasia is a hereditary disorder of ectodermthat involvesteeth, skin, and hair, nails, salivary, lacrimal and sweat glands. The most common type of diseaseishypohydrotic ectodermal dysplasia that is inherited as recessive x-linked trait.
The main clinical symptoms are dry skin, sparse thinhair, small brittle nails, hyperkeratosis of palms and soles, complete or partial missing of sweat glands, hypodontia and oligodontia.
Case report:The patient was a six years oldfemalewith hypohydrotic ectodermal dysplasia with the chief complaint of difficult eating. The clinical and radiographic examinations showed conical teeth and microdontia, hypodontia, increased overbite, and atrophic alveolar ridge. The oral rehabilitation was performed by constructing overdentures on both jaws.The oral functions including mastication, speaking and esthetics were improved to a large extent.
Key words: HypohydroticEctodermal dysplasia, Oral rehabilitation, Removable denture
Type of Article: Research Article | Subject: General
Received: 2017/08/20 | Accepted: 2017/08/20 | Published: 2017/08/20

References
1. Visinoni A.F, Lisboa-Costa T, Pagnan N.A, etc. Ectodermal dysplasias: clinical and molecular review. Am. J. Med. Genet. A. 2009;149A:1980–2002. doi: 10.1002/ajmg.a.32864. [DOI:10.1002/ajmg.a.32864]
2. Freire-Maia N. Ectodermal dysplasias. Hum. Hered. 1971;21:309–312. doi: 10.1159/000152419. [DOI:10.1159/000152419]
3. Nguyen-Nielsen M, Skovbo S, Svaneby D, Pedersen L, etc. The prevalence of X-linked hypohidrotic ectodermal dysplasia (XLHED) in Denmark, 1995–2010. Eur J Med Genet. 2013 May;56(5):236-42. [DOI:10.1016/j.ejmg.2013.01.012]
4. Vieira K.A, Teixeira M.S, Guirado C.G, etc. Prosthodontic treatment of hypohidrotic ectodermal dysplasia with complete anodontia: Case report. Quintessence Int. 2007;38:75–80.
5. De Aquino S.N, Paranaiba L.M, Swerts M.S, Martelli D.R, de Barros L.M, Martelli Junior H. Orofacial features of hypohidrotic ectodermal dysplasia. Head Neck Pathol. 2012 Dec;6(4):460-6. [DOI:10.1007/s12105-012-0349-4]
6. Kutkowska-Kaźmierczak A, Niepokój K, Wertheim-Tysarowska K. et al. J Appl Genetics. 2015; 56: 329. doi:10.1007/s13353-014-0266-1. [DOI:10.1007/s13353-014-0266-1]
7. Tarjan I, Gabris K, Rozsa N. Early prosthetic treatment of patients with ectodermal dysplasia: a clinical report. jprosthet dent. 2005;93:419–24. [DOI:10.1016/j.prosdent.2005.01.012]
8. Nunn J.H, Carter N, Gillgrass T, etc. The interdisciplinary management of hypodontia: background and role of paediatric dentistry. br dent j. 2003;194:245–51. [DOI:10.1038/sj.bdj.4809925]
9. Pagnan N.A., Visinoni A.F. Update on ectodermal dysplasias clinical classification. Am. J. Med. Genet. A. 2014;164A:2415–2423. doi: 10.1002/ajmg.a.36616. [DOI:10.1002/ajmg.a.36616]
10. Osborn J.F. Die alveolar extensions plastik. Teil I. Quintessence. 1985;36:9–16.
11. Zeng B, Lu H, Xiao X, etc. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation. Oral Dis. 2015;21:994–1000. doi: 10.1111/odi.12376. [DOI:10.1111/odi.12376]
12. Deshmukh S., Prashanth S. Ectodermal dysplasia: a genetic review. Int. J. Clin. Pediatr. Dent. 2012;5:197–202. doi: 10.5005/jp-journals-10005-1165. [DOI:10.5005/jp-journals-10005-1165]
13. Lo muzio l, Bucci P, Carile F, et al. Prosthetic rehabilitation of a child affected from anhydrotic ectodermal dysplasia: a case report. jcontemp dent pract. 2005;6:120–6.
14. Buyse M.L. Birth defects encyclopedia. pp 597–8. Chicago-St Louis: Mosby, 1990.
15. VasconcelosCarvalho M, Romero Souto de Sousa J, Paiva Correa de Melo F, et al. Hypohidrotic and hidrotic ectodermal dysplasia: A report of two cases. Dermatol Online J. 2013;19:18985.
16. Koyuncuoglu C.Z, Metin S, Saylan I, etc. Full-mouth rehabilitation of a patient with ectodermal dysplasia with dental implants. J Oral Implantol. 2014;6:714–21. [DOI:10.1563/AAID-JOI-D-12-00072]
17. Carvalho M.V, De Sousa J.R.S, De Melo F. P. C. et al. Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases. Dermatology Online J. 2013;19:18985.
18. Derbanne M.A, Sitbon M.C, Landru M.M, etc. Case report: Early prosthetic treatment in children with ectodermal dysplasia. Eur Arch Paediatr Dent. 2010 Dec;11(6):301-5. [DOI:10.1007/BF03262768]
19. Kearns G, Sharma A, Perrott D, etc. Placement of endosseous implants in children and adolescents with hereditary ectodermal dysplasia. Oral Surg Oral Med Oral Pathol Oral RadiolEndod. 1999 Jul;88(1):5-10. [DOI:10.1016/S1079-2104(99)70185-X]
20. Sweeney I.P, Ferguson J.W, Heggie A.A, etc. Treatment outcomes for adolescent ectodermal dysplasia patients treated with dental implants. Int J Paediatr Dent. 2005 Jul;15(4):241-8. [DOI:10.1111/j.1365-263X.2005.00610.x]
21. De Alencar N.A, Reis K.R, Antonio A.G, etc. Influence of oral rehabilitation on the oral health-related quality of life of a child with ectodermal dysplasia. J Dent Child (Chic). 2015 Jan-Apr;82(1):36-40.
22. Imirzalioglu P, Uckan S, Haydar S.G. Surgical and prosthodontic treatment alternatives for children and adolescents with ectodermal dysplasia: a clinical report. jprosthet dent. 2002;88:569–72. [DOI:10.1067/mpr.2002.130146]
23. Rad A.S, Siadat H, Monzavi A, Mangoli A.A. Full mouth rehabilitation of a hypohidrotic ectodermal dysplasia patient with dental implants: a clinical report. jprosthodont. 2007;16:209–13. [DOI:10.1111/j.1532-849X.2006.00173.x]
24. Murdock S, Lee J.Y, Guckes A, etc. A costs analysis of dental treatment for ectodermal dysplasia. J am dent assoc. 2005;136:1273–6. [DOI:10.14219/jada.archive.2005.0343]
25. Ramos V, Giebink D.L, Fisher J.G, Christensen L.C. Complete dentures for a child with hypohidrotic ectodermal dysplasia: a clinical report. jprosthet dent. 1995;74:329–31. [DOI:10.1016/S0022-3913(05)80369-5]
26. Shaw R.M. Prosthetic management of hypohidrotic ectodermal dysplasia with anodontia case report. aust dent j. 1990;35:113–6. [DOI:10.1111/j.1834-7819.1990.tb05873.x]
27. Franchi L, Branchi R, Tollaro I. Craniofacial changes following early prosthetic treatment in a case of hypohidrotic ectodermal dysplasia with complete anodontia. asdc j dent child. 1998;65:116–21.

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