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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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Bibliografische gegevens
Gepubliceerd in:BJR Case Rep
Hoofdauteurs: Jagtap, Rohan, Srivastava, Ambika, Jadhav, Aniket, Gupta, Swati
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The British Institute of Radiology. 2020
Onderwerpen:
Online toegang: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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