Waardenburg Syndrome Report
Waardenburg Syndrome
Characterized by differing levels of hearing impairment and minor structural abnormalities originating from the neural crest, Waardenburg Syndrome (WS) results in irregular pigmentation of the eyes, hair, and skin. WS manifests in four distinct clinical and genetic phenotypes. There is currently no known cure for Waardenburg Syndrome, but individuals with this condition typically have a normal life expectancy and can lead fulfilling lives. However, it is essential to address and manage any symptoms as they arise.
8 genes genes analyzed
It is recommended if:
This report is appropriate for individuals who show clinical indications, symptoms, or have familial suspicions of Waardenburg Syndrome.
List of main conditions:
- Waardenburg syndrome, type 4A
- Waardenburg syndrome, type 4B
- Waardenburg syndrome, type 1
Simple workflow
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