![Waardenburg Syndrome (Gentics and Communication Disorders Series) by Kahn, Alice 9781597560214 | eBay Waardenburg Syndrome (Gentics and Communication Disorders Series) by Kahn, Alice 9781597560214 | eBay](https://i.ebayimg.com/images/g/TXgAAOSwsEdjszjz/s-l500.jpg)
Waardenburg Syndrome (Gentics and Communication Disorders Series) by Kahn, Alice 9781597560214 | eBay
![Image is unedited) This child has a rare genetic disorder called Waardenburg syndrome. Symptoms include streaks of white hair, deafness, and extremely blue eyes. : r/interestingasfuck Image is unedited) This child has a rare genetic disorder called Waardenburg syndrome. Symptoms include streaks of white hair, deafness, and extremely blue eyes. : r/interestingasfuck](https://external-preview.redd.it/NUEuQvD2G0XLj-9gf82zslaBRt-ZStUyul1VghG3n-Q.jpg?auto=webp&s=2aab7e08eba5a865ca2a5daad2fd946bafe5b2dc)
Image is unedited) This child has a rare genetic disorder called Waardenburg syndrome. Symptoms include streaks of white hair, deafness, and extremely blue eyes. : r/interestingasfuck
![A de novo deletion mutation in SOX10 in a Chinese family with Waardenburg syndrome type 4 | Scientific Reports A de novo deletion mutation in SOX10 in a Chinese family with Waardenburg syndrome type 4 | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep41513/MediaObjects/41598_2017_Article_BFsrep41513_Fig1_HTML.jpg)
A de novo deletion mutation in SOX10 in a Chinese family with Waardenburg syndrome type 4 | Scientific Reports
What is the simplest explanation for the cause of Waardenburg syndrome? Why can it not be cured? - Quora
Raising a child with Waardenburg syndrome | What's it like to raise a child with Waardenburg syndrome? This Ghanaian mother shares her experience: | By BBC World Service | Facebook
![Targeted next-generation sequencing identified a novel variant of SOX10 in a Chinese family with Waardenburg syndrome type 2 - Xiao-Wen Liu, Su-Yang Wang, Zhan-Kui Xing, Yi-Ming Zhu, Wen-Juan Ding, Lei Duan, Xiao Targeted next-generation sequencing identified a novel variant of SOX10 in a Chinese family with Waardenburg syndrome type 2 - Xiao-Wen Liu, Su-Yang Wang, Zhan-Kui Xing, Yi-Ming Zhu, Wen-Juan Ding, Lei Duan, Xiao](https://journals.sagepub.com/cms/10.1177/0300060520967540/asset/images/large/10.1177_0300060520967540-fig1.jpeg)