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1.
Med J Malaysia ; 62(3): 238-40, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18246915

RESUMEN

This study was designed to identify surface and subsurface microscopic changes in different carious lesions by using Confocal Laser Scanning Microscope (CLSM) and Image analyzer (light microscopy). Thirty extracted carious posterior teeth were fixed, embedded and polymerized in plastic fixation medium. The final thin sections (80mm) were stained with H&E and Masson Goldner's Tricome while others were left unstained. Under Confocal, marked differences between control sound enamel and dentin, and carious area of the samples were observed which illustrated that a correlation existed between the zone of autofluoresence, demineralization and carious enamel and dentin. Compared to CLSM, Image Analyzer only produce two-dimensional images but the histopathological changes were better appreciated by using various staining methods.


Asunto(s)
Caries Dental , Esmalte Dental , Procesamiento de Imagen Asistido por Computador , Microscopía Confocal , Humanos
2.
J Clin Pediatr Dent ; 28(4): 319-22, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15366620

RESUMEN

Amelogenesis imperfecta (AI) is a hereditary disorder resulting in generalized defects in the enamel. The case reported here is of a seven-year-old male child with yellow color of all his teeth. Two of his primary molars were extracted due to dental abscess with advanced root resorption. Histologically hypoplastic enamel layer, positively birefringent, generalized pitting, roughness with irregular general cracked borders were observed. Scanning electron microscope, revealed extensive irregular, disorganized rough superficial enamel layer. The enamel was irregularly decussate with filamentous prisms accompanied by small rounded formations. The morphological and histological examination of the tooth revealed that this patient has the features of AI. For genetic study blood sample were collected from the patient and PCR analysis revealed that there is no mutation in exons 1-7 of AMELX gene on the X chromosome of the patient. Hence, it is probable that the AI of this patient is not X-linked. It is more likely to be an autosomal mutation.


Asunto(s)
Amelogénesis Imperfecta/patología , Esmalte Dental/ultraestructura , Amelogénesis Imperfecta/genética , Niño , Cromosomas Humanos X/genética , Hipoplasia del Esmalte Dental/patología , Exones/genética , Humanos , Masculino , Microscopía Electrónica de Rastreo , Diente Molar/ultraestructura , Mutación/genética , Diente Primario/ultraestructura
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