Waardenburg syndrome, an autosomal dominant genetic condition, presents a constellation of congenital anomalies ranging from hearing loss to distinctive hair and facial characteristics. To ensure optimal patient care, healthcare providers need to understand the intricacies of this syndrome.
What is Waardenburg Syndrome?
Waardenburg syndrome is a genetic disorder often characterised by varying degrees of deafness, minor defects in structures arising from the neural crest, and pigmentation...
