2018, Number 1
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Rev Odont Mex 2018; 22 (1)
Dental handling of patients with Christ-Siemens-Touraine syndrome. Case report
Orozco PJ, Puello CC, Hernández GD, Rovira OCJ
Language: Spanish
References: 17
Page: 51-55
PDF size: 213.39 Kb.
ABSTRACT
Ectodermal dysplasia (ED) encompasses a group of hereditary disorders in which two or more ectoderm-derived structures are affected. Patients afflicted with this disorder exhibit hypoplasia or aplasia of different structures such as skin, hair, nails, teeth, and sweat glands among others. Dental treatment is of the utmost importance in order to improve the subject’s quality of life. The case here reported depicts a male patient affected with Christ-Siemens-Touraine syndrome, who sought treatment due to tooth anodontia in upper and lower jaws. A dental approach was conducted involving periodontal treatment, oral rehabilitation and implantology, a social component was also furthered, directed to re-establish function and esthetics of the stomatognatic system. Performed treatment achieved absolute improvement in the masticatory process and esthetic smile which was satisfactory for the patient and his legal representative.
REFERENCES
Vasconcelos CM, Romero SS, Paiva CM, Fonseca FT, Nunes SA, Carvalho S et al. Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases. Dermatol Online J. 2013; 19 (7): 18985.
Jananee J, Satishkumar M, Balaji S. Ectodermal dysplasia-a case report. Indian J Multidiscip Dent. 2012; 2: 465-467.
Masís PC, Montero SO, Gomez FA. Diagnóstico y manejo odontológico del paciente infantil con displasia ectodérmica anhidrótica: Síndrome de Christ Siemens Touraine. Rev Cient Odontol. 2010; 6 (1): 14-19.
Marín BM, Espinal BG, Arroyo FT, Posso ZM, David PM, Castañeda PD, Sierra PJ. Displasia ectodérmica hipohidrótica: Reporte de casos. Av Odontoestomatol. 2013; 29 (1): 11-23.
Wright JT, Morris C, Clements SE, D’Souza R, Gaide O, Mikkola M et al. Classifying ectodermal dysplasias: incorporating the molecular basis and pathways. Am J Med Genet A. 2009; 149A (9): 2062-2067.
Shigli AN SP. Prosthodontic management of patients with Christ-Siemens-Touraine syndrome. BMJ Case Rep. 2012; 10: 1-7.
Jalili VP, Neema HC. Ectodermal dysplasia. A cephalometric appraisal. J Pierre Fauchard Acad. 2013; 27 (2): 41-48.
Alves N, De Oliveira RJ, Figueiredo ND. Displasia ectodérmica hidrótica. Un síndrome de interés para la odontología. Int J Odontostomat. 2012; 6 (1): 45-50.
Nascimento SA, Ribeiro LM, Oliveira MS, Barbosa DS, Barros ML, Júnior MH. Orofacial features of hypohidrotic ectodermal dysplasia. Head Neck Pathol. 2012; 6 (4): 460-466.
Vallejo PA, López-Arranz ME, González GM. Tratamiento odontológico en la displasia ectodérmica: actualización. Av Odontoestomatol. 2006; 22 (3): 171-176.
García-Martín P, Hernández-Martín A, Torrelo A. Displasias ectodérmicas : revisión clínica y molecular. Actas Dermo-Sifiliográficas. 2016; 104 (6): 451-470.
Mokhtari S, Mokhtari S, Lotfi A. Christ-siemens-touraine syndrome: a case report and review of the literature. Case Rep Dent. 2012: 586418.
Kishore M, Panat SR, Aggarwal A, Agarwal N, Upadhyay N, Ajai K et al. Hypohidrotic ectodermal dyplasia: a case series. J Clin Diagn Res. 2014; 8 (1): 273-275.
Halai T, Stevens C. Ectodermal dysplasia: a clinical overview for the dental practitioner. Dent Update. 2015; 42 (8): 779-780, 783-784, 787-788.
Maroulakos G, Artopoulou II, Angelopoulou MV, Emmanouil D. Removable partial dentures vs overdentures in children with ectodermal dysplasia: two case reports. Eur Arch Paediatr Dent. 2015; 17 (3): 205-210.
Report C. Hypohidrotic ectodermal dysplasia: prosthetic and endodontic management. Int J Clin Pediatr Dent. 2010; 3 (1): 63-67.
Vilanova LS, Sánchez-Ayala A, Ribeiro GR, Campos CH, Farias-Neto A. Conventional complete denture in patients with ectodermal dysplasia. Case Rep Dent. 2015; 2015: 714963.