0000000000547909

AUTHOR

Josep Maria Ustrell-torrent

showing 2 related works from this author

An epidemiological study of dental agenesis in a primary health area in Spain : estimated prevalence and associated factors

2010

Objectives: To evaluate the prevalence of dental agenesis and its possible association with other developmental dental anomalies and systemic entities. Setting and Sample Population: Descriptive transversal study, for which 1518 clinical records, of patients visited by the Odontological Service of the Primary Health Centre of Cassà de la Selva (Girona-Spain) between December 2002 and February 2006 were reviewed. The data were recorded in relation to the oral and dental anomalies and the associated systemic entities, between the ones referred as concomitant in literature. Results: Values of 9.48% (7.25% excluding the third molars) for dental agenesis and 0.39% for oligodontia were obtained. …

MalePediatricsmedicine.medical_specialtyCataloniaDentistryCentres d'atenció primàriaOligodontia03 medical and health sciences0302 clinical medicinePatologia dentalCatchment Area Healthstomatognathic systemGenetic etiologyRisk FactorsPrimary healthEpidemiologymedicinePrevalenceDentitionHumansEspanyaGeneral Dentistry030304 developmental biologyAnodontia0303 health sciencesDental anomaliesPrimary Health Carebusiness.industryDental agenesisCatalunyaCommunity health services030206 dentistryDentició:CIENCIAS MÉDICAS [UNESCO]3. Good healthstomatognathic diseasesOtorhinolaryngologySpainConcomitantUNESCO::CIENCIAS MÉDICASSurgeryFemalebusinessClinical recordDental pathology
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Oral findings in Midline Syndrome: a case report and literature review

2010

We describe a female patient with a midline syndrome. The patient presents agenesis of the corpus callosum, encephalocele, iris coloboma, hypertelorism, submucosal cleft palate and dental anomalies. Despite being very characteristic, her phenotypical traits do not coincide exactly with those reported to date in the literature. The karyotype and the molecular cytogenetic study do not show mutations. We identify the presence of dental anomalies in the mother and other family members, not being identified MSX1 and PAX9 mutations that could the related with their etiology. Despite the fact that dental agenesis has been related to a large number of other malformation syndromes and congenital con…

medicine.medical_specialtyIrisEncephalocele03 medical and health sciences0302 clinical medicinestomatognathic systemMidline syndromeDental abnormalitiesmedicineHumansAbnormalities MultipleHypertelorismChildAgenesis of the corpus callosumGeneral DentistryEncephalocele030304 developmental biology0303 health sciencesHypertelorismTooth Abnormalitiesbusiness.industryDental agenesisSyndrome:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseDermatologyIris coloboma3. Good healthSurgeryCleft PalateColobomastomatognathic diseasesPhenotypeOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASEtiologyFemaleSurgeryMalformacionsAgenesis of Corpus Callosummedicine.symptombusinessMalformacions dentalsHuman abnormalitiesPAX9030217 neurology & neurosurgery
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