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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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Foilsithe in:Dent Res J (Isfahan)
Main Authors: Raviraj, Jayam, Suman, Venkata, Suresh, Dirasantchu, Kartik, K.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Medknow Publications & Media Pvt Ltd 2017
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5504876/
https://ncbi.nlm.nih.gov/pubmed/28702065
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