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Achondroplasia with multiple supplemental supernumerary teeth and multiple talon cusps: A rare case report
Achondroplasia is the most common cause of dwarfism, which is inherited as an autosomal dominant disorder, caused by genetic mutation in fibroblast growth factor 3, leading to defective maturation of chondrocytes. It is known to be associated with various oral and dental manifestations such as delay...
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| Udgivet i: | Dent Res J (Isfahan) |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5504876/ https://ncbi.nlm.nih.gov/pubmed/28702065 |
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