Waardenburg syndrome

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Waardenburg syndrome

Waardenburg syndrome (WS) is a disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest including pigmentation anomalies of eyes hair and skin. WS is classified into four clinical and genetic phenotypes.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version February 2024

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Waardenburg syndrome?

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Clinical Trials

For a list of clinical trials in this disease area, please click here.