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Dentin Dysplasia

More information in Books or onNLM PubMed
Definition: An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)  a tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES    Other names Dysplasias, Dentin; Dysplasia, Dentin; Dentin Dysplasias
 
SubstanceCAS Registry & nameCategoriesSource
Dentin dysplasia, type 1  0   *Dentin Dysplasia.
Dentin dysplasia, coronal  0   *Amelogenesis Imperfecta *Dentin Dysplasia.
Dentin dysplasia sclerotic bones  0   *Dentin Dysplasia Bone and Bones/abnormalities.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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