Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , |
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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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 |
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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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1813546414622375936 |