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Article

Waardenburg Syndrome type 1: A case report.

Dermatology online journal - 15 Nov 2011

Demirci Gulsen Tukenmez, Atıs Guldehan, Altunay Ilknur Kıvanc

Abstract excerpt

Waardenburg Syndrome (WS) is a rare hereditary disorder that is characterized by the clinical manifestations of oculocutaneous anomalies of pigmentation, congenital deafness, dystopia canthorum, and broad nasal root. It demonstrates both genetically and clinically heterogenous characteristics. In this article, we report an 11-month-old boy with WS1, one of four clinicat types of WS. He exhibited white forelock,...

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PMID: 22136859

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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