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Oral manifestation of Waardenburg syndrome: a case report and review of the literature
Waardenburg syndrome is a rare autosomal dominant genetic disorder of neural crest cell migration. It is characterized by congenital sensorineural hearing loss, heterochromia iridis, depigmentation of hair and skin, and increased intercanthal distance. It is subdivided into four subtypes with I and...
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| 出版年: | BJR Case Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The British Institute of Radiology.
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7709062/ https://ncbi.nlm.nih.gov/pubmed/33299596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1259/bjrcr.20200071 |
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