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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...

詳細記述

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書誌詳細
出版年:BJR Case Rep
主要な著者: Jagtap, Rohan, Srivastava, Ambika, Jadhav, Aniket, Gupta, Swati
フォーマット: Artigo
言語:Inglês
出版事項: The British Institute of Radiology. 2020
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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