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Treacher Collins syndrome: a case report
Treacher Collins syndrome is a rare autosomal dominant disorder of craniofacial development. The fully expressed phenotype exhibits characteristic dysmorphic features involving the face, eyes, mandible and ears. We report a case of a 17-year-old woman presenting with the typical orofacial implicatio...
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| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Publishing Group
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3669902/ https://ncbi.nlm.nih.gov/pubmed/23709540 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-009341 |
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