Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología

Detalhes bibliográficos
Autor(a) principal: Alves, Nilton [UNESP]
Data de Publicação: 2012
Outros Autores: Oliveira, Reinaldo José de, Figueiredo Deana, Naira
Tipo de documento: Artigo
Idioma: spa
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000100006
http://hdl.handle.net/11449/125826
Resumo: Hypohidrotic ectodermal dysplasia (HED) is a rare disease of genetic etiology. The most frequent form is of recessive linked to X-chromosome inheritance with affected male and female carriers. It can occur through autosomal mutations, of the gene EDA1 gene being responsible for the majority of the cases. It is characterized by the triad: hypohidrosis, oligodontia and hypotrichosis. We present two cases of patients with HED in which we observed characteristic signs of this syndrome: delicate skin, sparce hair, eyebrows and eyelashes, periorbital wrinkles, perioral and periorbital hyperpigmentation, prominent lips, in addition the patient in case 2 also present the depressed nasal bridge. We also found decreased salivary and lacrimal secretion and maxillary hypoplasia in both cases. At the oral examination in case 1 the upper right and left deciduous canines and lower right deciduous canine were present, and in case 2 the upper and lower (right and left) deciduous canines and two upper (one right and other left) permanent incisors were present with altered morphology, all of these dental elements were healthy. The early dental treatment of patients with HED, especially in the presence of oligodontia, as observed in our cases, is important not only to provide a better quality of life for these patients in the short term, but also an attempt to minimize the changes in facial growth to which these patients are subject.
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spelling Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontologíaHypohidrotic ectodermal dysplasia: a syndrome of interest to dentistryHypohidrotic ectodermal dysplasiaOligodontiaChrist-Siemens Touraine syndromeDisplasia ectodérmica hipohidróticaOligodonciaSíndrome de Christ-Siemens-TouraineHypohidrotic ectodermal dysplasia (HED) is a rare disease of genetic etiology. The most frequent form is of recessive linked to X-chromosome inheritance with affected male and female carriers. It can occur through autosomal mutations, of the gene EDA1 gene being responsible for the majority of the cases. It is characterized by the triad: hypohidrosis, oligodontia and hypotrichosis. We present two cases of patients with HED in which we observed characteristic signs of this syndrome: delicate skin, sparce hair, eyebrows and eyelashes, periorbital wrinkles, perioral and periorbital hyperpigmentation, prominent lips, in addition the patient in case 2 also present the depressed nasal bridge. We also found decreased salivary and lacrimal secretion and maxillary hypoplasia in both cases. At the oral examination in case 1 the upper right and left deciduous canines and lower right deciduous canine were present, and in case 2 the upper and lower (right and left) deciduous canines and two upper (one right and other left) permanent incisors were present with altered morphology, all of these dental elements were healthy. The early dental treatment of patients with HED, especially in the presence of oligodontia, as observed in our cases, is important not only to provide a better quality of life for these patients in the short term, but also an attempt to minimize the changes in facial growth to which these patients are subject.La displasia ectodérmica hipohidrótica (DEH) es una enfermedad rara de etiología genética. La forma más frecuente es la de herencia recesiva relacionada al cromosomo X con sujetos de sexo masculino afectados y de sexo femenino portadores. Pueden ocurrir a través de mutaciones autosómicas, y en estas, las del gene EDA1 son responsables por la mayoría de los casos. Se caracteriza por la tríada: hipohidrosis, oligodoncia e hipotricosis. Presentamos dos casos de pacientes con DEH en los cuales se observaron signos característicos del síndrome: piel delicada; cabellos, cejas y pestañas escasos; arrugas periorbitales; hiperpigmentación perioral y periorbital; labios prominentes y además de eso el paciente del caso 2 presentaba depresión del puente nasal. Se constató aún disminución de la secreción salival y lagrimal y hipoplasia de maxila en los dos casos. Al examen oral estaban presentes en el caso 1 los caninos superiores derecho e izquierdo temporales y el canino inferior derecho temporal y en el caso 2 los caninos superiores e inferiores (derechos e izquierdos) temporales y dos incisivos superiores (uno derecho y otro izquierdo) permanentes con morfología alterada, siendo todos los elementos dentarios íntegros. El tratamiento odontológico precoz de los portadores de DEH, principalmente en la presencia de oligodoncia, como la que se observa en los casos aquí reportados, es importante no solamente para ofrecer mejor calidad de vida para estos pacientes en corto plazo, sino también en el intento de mitigar las alteraciones en el crecimiento facial a que estos pacientes están sometidos.Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Odontologia de Araraquara, Araraquara, Rua Humaitá,1680 - Departamento de Morfologia, Centro, CEP 14801-903, SP, BrasilUniversidade Estadual Paulista (Unesp)niversidade Bandeirante de São Paulo (UNIBAN)Alves, Nilton [UNESP]Oliveira, Reinaldo José deFigueiredo Deana, Naira2015-08-06T16:13:13Z2015-08-06T16:13:13Z2012info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article45-50application/pdfhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000100006International Journal of Odontostomatology, v. 6, n. 1, p. 45-50, 2012.0718-3801http://hdl.handle.net/11449/12582610.4067/S0718-381X2012000100006ISSN0718-3801-2012-06-01-45-50.pdf6822070436128193Currículo Lattesreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPspaInternational Journal of Odontostomatologyinfo:eu-repo/semantics/openAccess2024-09-27T15:14:57Zoai:repositorio.unesp.br:11449/125826Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T15:14:57Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
Hypohidrotic ectodermal dysplasia: a syndrome of interest to dentistry
title Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
spellingShingle Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
Alves, Nilton [UNESP]
Hypohidrotic ectodermal dysplasia
Oligodontia
Christ-Siemens Touraine syndrome
Displasia ectodérmica hipohidrótica
Oligodoncia
Síndrome de Christ-Siemens-Touraine
title_short Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
title_full Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
title_fullStr Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
title_full_unstemmed Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
title_sort Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
author Alves, Nilton [UNESP]
author_facet Alves, Nilton [UNESP]
Oliveira, Reinaldo José de
Figueiredo Deana, Naira
author_role author
author2 Oliveira, Reinaldo José de
Figueiredo Deana, Naira
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
niversidade Bandeirante de São Paulo (UNIBAN)
dc.contributor.author.fl_str_mv Alves, Nilton [UNESP]
Oliveira, Reinaldo José de
Figueiredo Deana, Naira
dc.subject.por.fl_str_mv Hypohidrotic ectodermal dysplasia
Oligodontia
Christ-Siemens Touraine syndrome
Displasia ectodérmica hipohidrótica
Oligodoncia
Síndrome de Christ-Siemens-Touraine
topic Hypohidrotic ectodermal dysplasia
Oligodontia
Christ-Siemens Touraine syndrome
Displasia ectodérmica hipohidrótica
Oligodoncia
Síndrome de Christ-Siemens-Touraine
description Hypohidrotic ectodermal dysplasia (HED) is a rare disease of genetic etiology. The most frequent form is of recessive linked to X-chromosome inheritance with affected male and female carriers. It can occur through autosomal mutations, of the gene EDA1 gene being responsible for the majority of the cases. It is characterized by the triad: hypohidrosis, oligodontia and hypotrichosis. We present two cases of patients with HED in which we observed characteristic signs of this syndrome: delicate skin, sparce hair, eyebrows and eyelashes, periorbital wrinkles, perioral and periorbital hyperpigmentation, prominent lips, in addition the patient in case 2 also present the depressed nasal bridge. We also found decreased salivary and lacrimal secretion and maxillary hypoplasia in both cases. At the oral examination in case 1 the upper right and left deciduous canines and lower right deciduous canine were present, and in case 2 the upper and lower (right and left) deciduous canines and two upper (one right and other left) permanent incisors were present with altered morphology, all of these dental elements were healthy. The early dental treatment of patients with HED, especially in the presence of oligodontia, as observed in our cases, is important not only to provide a better quality of life for these patients in the short term, but also an attempt to minimize the changes in facial growth to which these patients are subject.
publishDate 2012
dc.date.none.fl_str_mv 2012
2015-08-06T16:13:13Z
2015-08-06T16:13:13Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000100006
International Journal of Odontostomatology, v. 6, n. 1, p. 45-50, 2012.
0718-3801
http://hdl.handle.net/11449/125826
10.4067/S0718-381X2012000100006
ISSN0718-3801-2012-06-01-45-50.pdf
6822070436128193
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000100006
http://hdl.handle.net/11449/125826
identifier_str_mv International Journal of Odontostomatology, v. 6, n. 1, p. 45-50, 2012.
0718-3801
10.4067/S0718-381X2012000100006
ISSN0718-3801-2012-06-01-45-50.pdf
6822070436128193
dc.language.iso.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv International Journal of Odontostomatology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 45-50
application/pdf
dc.source.none.fl_str_mv Currículo Lattes
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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