A case of Waardenburg syndrome type I with congenital sensorineural hearing loss
AbstractWaardenburg syndrome is a rare genetic disorder characterized by hearing loss in association with pigmentary defects of the skin, hair and eyes. It is caused by the gene mutation involved in the development of melanocyte. A five years old, female child attended our hospital because of bilate...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Taylor & Francis Group
2023-12-01
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| Series: | Acta Oto-Laryngologica Case Reports |
| Subjects: | |
| Online Access: | https://www.tandfonline.com/doi/10.1080/23772484.2023.2221090 |