Dentofacial characteristics in a child with Meier–Gorlin syndrome: A rare case report

Meier–Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by the triad of microtia, absent or small patellae and short stature. The other associated clinical features may include developmental delay, congenital pulmonary emphysema, gastro-esophageal reflux, urogenital anomalie...

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Detalles Bibliográficos
Autores principales: Morankar, Rahul G., Goyal, Ashima, Gauba, Krishan, Kapur, Aditi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011216/
https://www.ncbi.nlm.nih.gov/pubmed/29942112
http://dx.doi.org/10.1016/j.sdentj.2018.04.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011216/
https://www.ncbi.nlm.nih.gov/pubmed/29942112
http://dx.doi.org/10.1016/j.sdentj.2018.04.004

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