{"id":13373,"date":"2024-08-23T00:40:40","date_gmt":"2024-08-22T22:40:40","guid":{"rendered":"https:\/\/valintermed.com\/?p=13373"},"modified":"2024-08-23T00:40:40","modified_gmt":"2024-08-22T22:40:40","slug":"sindrom-vaardenburga","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/vaardenburg-syndrome\/","title":{"rendered":"Waardenburg syndrome"},"content":{"rendered":"
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Waardenburg syndrome is a hereditary disorder characterized by changes in the pigmentation of the skin, hair, and eyes, as well as various hearing abnormalities. It belongs to a group of disorders associated with a deficiency of neuroblasts, which leads to defects in the development of melanocytes and structures responsible for hearing. The most characteristic manifestations of the syndrome are white or light blue hair, heterochromia (different-colored eyes), and a high probability of hearing loss. The syndrome was first described by scientist Peter Waardenburg in 1951 and has since remained the subject of active medical research.<\/p>\n

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