While Waardenburg syndrome is a rare genetic condition, the probability of passing it from parent to child is more likely. This mother and child are examples of this possibility.
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Ten people whose genes are not like the rest of us
The disease was first diagnosed in 1951 by DJ Waardenburg, an ophthalmologist. It is characterized by colored skin, irises of different colors, and in some cases, hearing loss and changes in vision.
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