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dc.contributor.CRUESPUNIVERSIDADE DE ESTADUAL DE CAMPINASpt_BR
dc.typeArtigo de periódicopt_BR
dc.titleKohlschütter-tönz Syndrome - Report Of An Additional Case.pt_BR
dc.contributor.authorGonzález-Arriagada, Wilfredo Apt_BR
dc.contributor.authorCarlos-Bregni, Románpt_BR
dc.contributor.authorContreras, Elisapt_BR
dc.contributor.authorAlmeida, Oslei Ppt_BR
dc.contributor.authorLopes, Marcio Apt_BR
unicamp.authorWilfredo A González-Arriagada, DDS, MSc. Oral Diagnosis Department, Semiology and Oral Pathology, Piracicaba Dental School, State University of Campinas (UNICAMP), Piracicaba, Sao Paulo, Brazilpt_BR
unicamp.authorOslei P Almeida, DDS, PhD. Oral Diagnosis Department, Semiology and Oral Pathology, Piracicaba Dental School, State University of Campinas (UNICAMP), Piracicaba, Sao Paulo, Brazil.pt_BR
unicamp.authorMarcio A Lopes, DDS, PhD. Oral Diagnosis Department, Semiology and Oral Pathology, Piracicaba Dental School, State University of Campinas (UNICAMP), Piracicaba, Sao Paulo, Brazil.pt_BR
unicamp.author.externalAssistant professor. Oral Pathology and Diagnosis, Facultad de Odontología, Universidad de Valparaíso, Valparaíso, Chile.pt
unicamp.author.externalRomán Carlos-Bregni, DDS. Oral Pathology Section, Centro Clínico de Cabeza y Cuello/Hospital Herrera Llerandi, Guatemala City, Guatemala.pt
unicamp.author.externalElisa Contreras, DDS. Oral Pathology Section, Centro Clínico de Cabeza y Cuello/Hospital Herrera Llerandi, Guatemala City, Guatemala.pt
dc.description.abstractKohlschütter-Tönz Syndrome is a rare disorder clinically characterized by amelogenesis imperfecta, epilepsy and progressive mental deterioration. We present an additional case of this syndrome of a nine year-old boy who was referred by pigmented teeth. The mental deterioration was associated with speech delay, impulsive behavior, attention-deficit/hyperactivity disorder, and learning problems. The physical examination revealed a reduction of lower third, slightly palpebral fissures, low ear and hair implantation, coarse hair and hypertrichosis. The intraoral examination showed alteration in teeth pigmentation diagnosed as amelogenesis imperfecta. Although rare, the present case report illustrates a syndrome that has dental anomalies and systemic alterations. It is important to recognize this syndrome as early as possible and paediatric dentist may contribute to the diagnosis and consequently to better manage the patients. Key words:Kohlschütter-Tönz syndrome, amelogenesis imperfecta, seizures, mental deterioration.en
dc.relation.ispartofJournal Of Clinical And Experimental Dentistrypt_BR
dc.relation.ispartofabbreviationJ Clin Exp Dentpt_BR
dc.date.issued2013-Aprpt_BR
dc.identifier.citationJournal Of Clinical And Experimental Dentistry. v. 5, n. 2, p. e108-11, 2013-Apr.pt_BR
dc.language.isoengpt_BR
dc.description.volume5pt_BR
dc.description.firstpagee108-11pt_BR
dc.rightsabertopt_BR
dc.rights.holderpt_BR
dc.sourcePubMedpt_BR
dc.identifier.issn1989-5488pt_BR
dc.identifier.doi10.4317/jced.51018pt_BR
dc.identifier.urlhttp://www.ncbi.nlm.nih.gov/pubmed/24455057pt_BR
dc.date.available2015-11-27T13:32:28Z-
dc.date.accessioned2015-11-27T13:32:28Z-
dc.description.provenanceMade available in DSpace on 2015-11-27T13:32:28Z (GMT). No. of bitstreams: 1 pmed_24455057.pdf: 353499 bytes, checksum: 0751950f91a09e9e9d30c10d134d4302 (MD5) Previous issue date: 2013en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/200954-
dc.identifier.idPubmed24455057pt_BR
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