M. CALLEA, F. FALETRA, A. MAESTRO, F. VERZEGNASSİ, M. RABUSİN, A. VİNCİGUERRA, F. RADOVİCH, G. CLARİCH, İ. YAVUZ, E. C. TUMEN

Dental Phenotype in a Patient with Hypoidrotıc Ectodermal Dysplasia and Severe Immunodeficiency

Anahtar Kelimeler:

-

Dental Phenotype in a Patient with Hypoidrotıc Ectodermal Dysplasia and Severe Immunodeficiency

Keywords:

-,

PDF

___

Clarke A. Hypohidrotic ectodermal dysplasia. J Med Genet 1987; 24(11):659-63.
Bonilla ED, Guerra L, Luna O. Overdenture prosthesis for oral rehabilitation of hypohidrotic ectodermal dysplasia: a case report. Quint Int 1997;28:657-665.
Tumen EC, Hamamcı N, Değer Y, Süer Tümen D, Agaçkiran E. Direct composite resin application, and prosthetic management in a patient with hypohidrotic ectodermal dysplasia: A case report. J Int Dent Med Res (JIDMR) 2009; 2(1), 19-24.
Yavuz I, Ulku SZ, Unlu G, Devecioglu KAMA , Kaya S, Adiguzel O, Akun Kaya F,Tumen EC, Zortuk M, Bashi E, Arslanoglu Z, “Ectodermal Dysplasia: Clinical Diagnosis”, International Dental and Medical Disorders 2008; 1, 1-10.
Adiguzel O, Kaya S, Yavuz I, Atakul F, “Oral Findings of Ectodermal Dysplasia and Literature Review”, International Dental and Medical Disorders, 2008; 1, 43-49.
Yavuz, I., Z. Baskan, R. Ulku, T.C. Dulgergil, O. Dari, A. Ece, Y. Yavuz ve O. Dari, “Ectodermal Dysplasia: Retrospective Study of 15 Cases,” Archives of Medical Research, 37(3), 403-409 (2006).
Levin LS. Dental and oral abnormalities in selected ectodermal dysplasia syndromes. Birth Defects Orig Artic Ser 1988;24:205-227. 8. Champlin TL, Mallory SB. Hypohidrotic ectodermal dysplasia: a review. J Ark Med Soc 1989;86:115-117.
Freire-Maia N, Pinheiro M. Ectodermal dysplasia: a clinical and genetic study. New York: Alan R. Liss;1984: 25-31.
Kere J, Srivastava AK, Montonen O, et al. X-linked anhidrotic (hipohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 1996;13:409-416.
Permaul P, Narla A, Hornick JL, Pai SY. Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes. Immunol Res 2009; 44(1-3): 89-98.
Roberts CM, Angus JE, Leach IH, McDermott EM, Walker DA, Ravenscroft JC. A novel NEMO gene mutation causing osteopetrosis, lymphoedema, hypohidrotic ectodermal dysplasia and immunodeficiency (OL-HED-ID). Eur J Pediatr 2010; 169(11): 1403-7.
Fish JD, Duerst RE, Gelfand EW, Orange JS, Bunin N. Challenges in the use of allogeneic hematopoietic SCT for ectodermal dysplasia with immune deficiency. Bone Marrow Transplant 2009; 43(3): 217-21. Epub 2008 Sep 15.
Răducanu AM, Păuna M, Feraru IV. A simple prosthetic restorative solution of a single peg-shaped upper central primary incisor in a case of ectodermal dysplasia. Rom J Morphol Embryol 2010; 51(2): 371-4.
Yavuz I, Kiralp S, Baskan Z. Hypohidrotic ectodermal dysplasia: a case report. Quint Int 2008; 39(1): 81-6.
Saw VP, Dart JK, Sitaru C, Zillikens D. Cicatrisig conjunctivitis with anti-basement membrane autoantibodies in ectodermal dysplasia Br J Ophthalmol 2008; 92(10):1403-10.