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Non-syndromic occurrence of multiple dental and skeletal anomalies: a rare case report and brief literature review.
MedLine Citation:
PMID:  25177656     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Oral physician has always been challenged when it comes to diagnosing rare nonsyndromic cases because of the varied presentation of multiple dental abnormalities caused due to mutations in developmental regulatory genes. This coupled with skeletal abnormalities makes the task more difficult. But as we come across such rare constellation of findings, it makes the field more intriguing. Here, we report an extremely rare case of non syndromic occurrence of dental manifestations like multiple dens invaginatus, generalised microdontia, generalised hypoplasia, hypodontia, pulp stones and widening of pulp chamber along with skeletal findings of bilateral syndactyly of legs and brachydactyly of hands and legs. Although many non syndromic cases have been reported in the literature, the unusual occurrence of findings in the present case is being reported for the first time.
Authors:
Santosh Patil; Nidhi Yadav; Prashant Patil
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Publication Detail:
Type:  Journal Article     Date:  2014-07-20
Journal Detail:
Title:  Journal of clinical and diagnostic research : JCDR     Volume:  8     ISSN:  2249-782X     ISO Abbreviation:  J Clin Diagn Res     Publication Date:  2014 Jul 
Date Detail:
Created Date:  2014-09-01     Completed Date:  2014-09-01     Revised Date:  2014-09-03    
Medline Journal Info:
Nlm Unique ID:  101488993     Medline TA:  J Clin Diagn Res     Country:  India    
Other Details:
Languages:  eng     Pagination:  ZD28-30     Citation Subset:  -    
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