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DeCS
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Descriptor English:
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Dentinogenesis Imperfecta
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Descriptor Spanish:
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Dentinogénesis Imperfecta
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Descriptor Portuguese:
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Dentinogênese Imperfeita
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Synonyms English:
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Hereditary Opalescent Dentin
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Tree Number:
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C07.650.800.270
C07.793.700.270
C16.131.850.800.270
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Definition English:
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An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth, ranging from dusky blue to brownish. The dentin is poorly formed with an abnormally low mineral content; the pulp canal is obliterated, but the enamel is normal. The teeth usually wear down rapidly, leaving short, brown stumps. (Dorland, 27th ed) |
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Indexing Annotation English:
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a dentin abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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History Note English:
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65
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Allowable Qualifiers English:
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Record Number:
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3826
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Unique Identifier:
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D003811
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Occurrence in VHL:
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Similar:
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DeCS SciELO LILACS LIS
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