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Article

Waardenburg syndrome--a case report.

Contact lens & anterior eye : the journal of the British Contact Lens Association - 1 Feb 2013

Bansal Yuvika, Jain Parul, Goyal Gaurav, Singh Malvika, Mishra Chittranjan

Abstract excerpt

Waardenburg syndrome is a rare genetic disorder characterized by varying degree of deafness associated with pigmentary anomaly and defects of neural crest cell derived structures. Four subtypes (I-IV) with variable penetrance and gene expression of different clinical features have been described. We report a patient showing constellation of complete heterochromia, dystopia canthorum, white forelock, and...

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Source

Identifiers

PMID: 23121842
DOI: 10.1016/j.clae.2012.10.083

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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