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Goldenhar Syndrome: A Case Report with Review
Goldenhar syndrome is a rare condition which is characterized by a multitude of anomalies involving craniofacial structures, vertebrae, internal organs and usually occurs unilaterally. The etiology of this syndrome is unclear since it varies genetically and is linked to a plethora of reasons. Herein...
Tallennettuna:
| Julkaisussa: | Int J Clin Pediatr Dent |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Jaypee Brothers Medical Publishers
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5086019/ https://ncbi.nlm.nih.gov/pubmed/27843263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1377 |
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