Waardenburg Syndrome

It is now accepted by doctors and the general public alike that Waardenburg syndrome is clearly associated with hearing loss. Not everyone with hearing loss has Waardenburg syndrome and not everyone with Waardenburg syndrome has hearing problems. However, there is a very clear correlation between the population of people with Waardenburg syndrome and the incidence of hearing loss. Since detecting Waardenburg syndrome is not always done by visual cues, it is often first detected when investigating a hearing deficit of a child.

While there are not proper symptoms of Waardenburg syndrome, there are some facial characteristics that many people associate with Klein Waardenburg syndrome. Some of these aspects often associated with Waardenburg syndrome are having two different colored eyes and having wideset eyes. Some people with the condition have blue eyes that of a shade of blue uncharacteristically seen.

Hearing Side

One of the biggest ways in which one can analyze a life affected by Klein Waardenburg syndrome is by looking at hearing loss. The genetic defect that goes the anomaly that is Waardenburg syndrome is often linked to a hearing loss. While researchers are still investigating this link, there is no question that the link exists. Since the condition is genetic, there is no cure for Waardenburg syndrome as yet, although finding the gene means that medicine is that much closer to isolating the gene for the purpose of rectifying the problems that can arise from Waardenburg syndrome.

Treatment

As a genetic defect, there are no treatments for Waardenburg syndrome in and of itself. There are ways to make life better and improve the quality of a life affected by Waardenburg syndrome, but there is currently no way to change the genetic code and prevent it from developing. If the genetic mutation is present, about half of the people will develop Waardenburg syndrome. Thus, the answer to the frequent question “is it reversible or stoppable Waardenburg syndrome,” is still a resounding ‘no’.

Support

Although cures do not exist, it is possible to find the Waardenburg syndrome foundation or support groups online, which can help one to deal with either the condition oneself or deal with caring for a loved one who has the syndrome. Klein Waardenburg syndrome pictures can be found online to help parents who are wondering if this is the condition that their child is presenting with; however, Waardenburg syndrome pictures online should be looked at knowing that this is no way to diagnose the condition; the pictures can give you an idea, only a doctor can give you a diagnosis.