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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...
Gorde:
| Argitaratua izan da: | Saudi Dent J |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Elsevier
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6011216/ https://ncbi.nlm.nih.gov/pubmed/29942112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.sdentj.2018.04.004 |
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