Buradasınız

EKTODERMAL DİSPLAZÎ (Bir Olgu Nedeoiyle)

ECTODERMAL DYSPLASIA ( A Case Report)

Journal Name:

Publication Year:

Keywords (Original Language):

Abstract (2. Language): 
Ectodermal dysplasia h a group of inherited disorders that orginates from various tissues of ectoderm. There arc two types of ectodermal dysplasia : Hypohidrotic and hidrotic. The most common form of ectodermal dysplasia is hypohidrotic ectodermal dysplasia, which most aiietLS LU G liaiU HtLllJ, ICtUI, SUIP mm ü.ıvuL ^.u-ıma. iiiv persons with anodontia / oligodontia caused by ectodermal dysplasia not only have difficulties in eating and speaking but can also sense that their appearance is different than others. An early diagnosis and treatment of dental problems of ectodermal dysplasia are important to improve esthetics and function. In this article , the clinical diagnosis of a sixteen years old girl with ectodermal dysplasia is evaluated and the common charactcristcs of ectodermal dysplasia is discussed. Full denture is fitted to patient to improve esthetics and function.
Abstract (Original Language): 
Eklûdermal Displazi* çeşitli ektodermal orijinli dokuların nadir görülen kalıtsal bir hastalığıdır, iki tipi vardır: Hidrotik vç hipohidrotik (anhidrotik), En sık görülen şekli saçları, deriyi, tırnaklan vc ter bezlerini etfcüeyen Hipohidrotik tiptir. Ektodermal displazinin sebep oîduğu oligodonti veya anadontili şahıslar konuşma ve yemek yemede güçlük çektikleri gibi diğer insanlardan farklı görünümleri ile daha duygusal olabilirler. Estetik ve fonksiyonu düzeltmek için ektodermal displazili hastaların dental problemlerinin erken teşhis ve tedavisi önem arzeder. Bu makalede kliniğimize başvuran 16 yaşında ektodermal displazili bir bayanın kîinik bulguları değerlendirildi ve hastalığın genel özelliklerinden bahsedildi. Hastanın çiğneme fonksiyonu ve estetiği total protez yapılarak sağlandı,
89-93

REFERENCES

References: 

l'Bakri H.RappR, Hadeedü.
Clinica
l management of ectodermal dysplasia. J Clin Pediatr Dent 1995; 19 (3): 167-72.
2- Bartslra TIL, Hulsmans R, Steijicn PM, ct id. Mosaic expression of hypohidrotic ectodermal dysplasia in an isolated affected female child. Arch Dermatol ]994;130 (ll):1421-4.
3- Bilge OM, Dayı E, Bocutoğlu Ö. Ectodermal Dyspl asi a: A case w i th im pac ted perma ne n t teeth. Australian Dent J 1995;40<4}: 229-32.
4- EHis RK, Donly KJ, Wild TW. Indirect composite resin crowns as an esthetic approach to treating ectodermal dysplasia: a case report. Quintessence Int I992;23 (İl):727-29.
5- Gordon CP, Litz S. Mtilticore myopathy in a patient with anhidrotic ectodermal dysplasia. Can .1 Anacslh 1992;39(9):966-8.
6- Guckes AD, Brahim JS, McCarthy GR> Rudy SF, Cooper LF. Using endosscous dental implants tor patients with ectodermal dysplasia, ,T Am Dent Assoc 1991;122:59-62.
7- Harorh A. Dig
Hekimliğ
i Radyolojisi. . Erzurum, 1992:166.
S-Koçak G, Gülhan A, Sandallı N. Ektodermal displazili bir çocuğun protetik ledavisi. 1st Dig Hek Fak Derg 1982;16(2):l3l-38,
9- Kupietzky A, Houpt M.
Hypohidroii
c ectodermal dysplasia; Characteristics and treatment. Quintessence Jnt I995;26(4):285-91.
10- Kücükiiçerlcr B. Pedodonti. Ankara, 197S:
265-66.
11- Nortje CJ, Farman AG, Thomas CH, Watermeyer GJJ, X-linkcd hypohidrotic ectodermal dysplasia-an unusual prosthetic problem. J Prosthct Dent 1978;40:137-42.
12- Özcan İ, Erdem T, Şirin S. Ektodermal dfcplazi (3 olgu nedeniyle), İst Diş Hck Fak Derg l991;25(l):i-5.
13- Pigno MA, Blackman RB, Cronin RJ, Cavazos E
Prosthodontic management of Ectodermal Dysplasia : A review of the literature. J Prosthct Dent 1996;76:541-45.
92
Atatürk Üniv .Diş Hek.Fak.Derg.
CilL:7 Sayı:! Sayfa: 89-93, 1997
YILMAZ, YANIKOGLU
14- Pinheiro M, Freire-Maia N.
Ectoderma
l dysplasias:A clinical classification and a causal review. Am J Med Genet 1994;53( 2): 153-62.
15- Ramos V, Gienbink DL, Fisher JG, Christensen LC. Complete dentures for a child with hypohidroiie ectodermal dysplasia: A clinical report. J prosthet Dent I995;74{4):329-31.
16- Renner RP, Kleinerman V. Overdenturc techniques in the management of oligodontia^ case report. Quintessence Int 1980;4:57-65.
f7-Shaw RM. Prosthetic management of hypohydrotk ectodermal dysplasia with anodontia:case report. Aust Dent J t990;35; L 3 3-16¬18 Smith RA, Vargervik K, Kearns G, Bosch C, KoumjİBfl J. Placement of an endosseous implant in growing child with ectodermal dysplasia. Oral Surg Oral Med Oral Pathol 1993;75:669-73.
19Tape MW, Tye E. Ectodermal dysplasia: Literature review and a case report. Compend Contin Educ Dent t995;16(5):524-8.
20- Ulusu T, Alaçam A, Iscan HN, Ucuncu N. Relation of ectodermal dysplasia and hypodontia. J Ctin Pediatr Dent 1990;I5(1):46-5Û.
21- Van Waas MA, Jonkman RE, Kalk W, Van11 Hof MA, Ptooij J, Van Os JH. Differences tvvn years after tooth extraction in mandibular bone reduction in patients treated with immediate overdentures or with immediate complete dentures. J Dent Res I993;72:1001-4.
22- Vierructi S, Bacetti T, Tollaro I. Dental and craniofacial findings in hypohidrotic ectodermal dysplasia during the primary dentition phase. J Clin Pediatr Dent 1994;I8(4):291 7.

Thank you for copying data from http://www.arastirmax.com