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Cornelia de Lange syndrome : a case report

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Cornelia de Lange syndrome : a case report

dc.contributor.author	Grau Carbó, Joaquím	es
dc.contributor.author	López Jiménez, Julián	es
dc.contributor.author	Giménez Prats, María José	es
dc.contributor.author	Sánchez Molins, Meritxell	es
dc.date.accessioned	2017-11-20T12:32:07Z
dc.date.available	2017-11-20T12:32:07Z
dc.date.issued	2007	es
dc.identifier.uri	http://hdl.handle.net/10550/63157
dc.description.abstract	Cornelia de Lange is a genetic syndrome which affects between 1/10.000 and 1/60.000 neonates, but its genetic bases are still not clear. Its principal clinical characteristics are the delay in growth and development, hirsute, structural anomalies in the limbs and distinctive facial characteristic. Dental problems are frequent and include: ogival palate, micrognathia, dental malalignment, delayed teething, microdontic teeth, periodontal disease and dental erosion produced by gastric reflux. Discussed is the case of a 29 year old patient affected by the syndrome in question, which presents the principal clinical characteristics. The patient?s general state of health is acceptable, without cardiac or respiratory alterations. The intraoral exploration shows policaries, periodontal disease, persistence of the temporal teeth and ectopic molars. After completing the necessary pre-operatory preparations, the entire odontological treatment was carried out under general aesthesia, due to the patient?s total lack of collaboration.	es
dc.source	Grau Carbó, Joaquím ; López Jiménez, Julián ; Giménez Prats, María José ; Sánchez Molins, Meritxell. Cornelia de Lange syndrome : a case report. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 12 6 2007: 7-	es
dc.title	Cornelia de Lange syndrome : a case report	es
dc.type	journal article	es_ES
dc.subject.unesco	UNESCO::CIENCIAS MÉDICAS	es
dc.identifier.doi		es
dc.type.hasVersion	VoR	es_ES