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1.
Surg Radiol Anat ; 38(9): 1099-1104, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26861010

RESUMEN

PURPOSE: Based on a case of supernumerary cusp on the bucca of left maxillary second molar diagnosed by cone beam computed tomography (CBCT), its genesis, diagnosis and antidiastole are to be analysed. The clinic implication of CBCT is correspondingly discussed. METHODS: The supernumerary cusp was diagnosed by oral general examination, intra-oral radiograph and CBCT. The features of supernumerary cusp, fused tooth, geminated tooth and concrescence tooth, especially differentiate points among them were discussed. RESULTS: The case of supernumerary cusp on the bucca of left maxillary second molar was diagnosed definitely by the combined application of oral general examination, periapical radiograph and CBCT. CONCLUSION: Supernumerary cusp on the bucca of left maxillary second molar is a rare phenomenon, which is difficult to be differentiated from other tooth deformities. CBCT can improve accuracy of diagnosis.


Asunto(s)
Tomografía Computarizada de Haz Cónico , Anomalías Dentarias/diagnóstico por imagen , Adulto , Humanos , Masculino , Radiografía Dental
2.
Am J Med Genet A ; 167A(11): 2830-3, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26250054

RESUMEN

SOX2 anophthalmia syndrome is an uncommon autosomal dominant syndrome caused by mutations in the SOX2 gene and clinically characterized by severe eye malformations (anophthalmia/microphthalmia) and extraocular anomalies mainly involving brain, esophagus, and genitalia. In this work, a patient with the SOX2 anophthalmia syndrome and exhibiting a novel dental anomaly is described. SOX2 genotyping in this patient revealed an apparently de novo c.70del20 deletion, a commonly reported SOX2 mutation. A review of the phenotypic variation observed in patients carrying the recurrent SOX2 c.70del20 mutation is presented. Although dental anomalies are uncommonly reported in the SOX2 anophthalmia syndrome, we suggest that a dental examination should be performed in patients with SOX2 mutations.


Asunto(s)
Atresia Esofágica/complicaciones , Microftalmía/complicaciones , Malformaciones del Sistema Nervioso/complicaciones , Anomalías Dentarias/complicaciones , Preescolar , Atresia Esofágica/genética , Humanos , Incisivo/diagnóstico por imagen , Recién Nacido , Masculino , Microftalmía/genética , Mutación , Malformaciones del Sistema Nervioso/genética , Radiografía , Factores de Transcripción SOXB1/genética , Anomalías Dentarias/diagnóstico por imagen , Anomalías Dentarias/genética
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