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Research Article Open access CC BY 4.0

Blue-Eyed Asian: A Case Report of Waardenburg Syndrome Type 1

Kris Zanna B. Acluba, Archimedes L. D. Agahan

Ophthalmology Research: An International Journal · pp. 1–5 · Published 15 Jan 2016

10.9734/OR/2016/23417

Abstract

Aims: To report a case of Waardeenburg Syndrome Type 1 presenting with bilateral blue iris in a young Asian. Presentation of Case: A 7-year old Filipino girl was referred for ophthalmologic evaluation for bilateral blue eyes. She also presented with an eyebrow flare, broad nasal root, dystopia canthorum, heterochromic fundi and mild hearing loss. Her medical, developmental and family histories were unremarkable. Discussion: Waardenburg Syndrome is a rare clinical disorder with oculocutaneous pigmentary anomalies, deafness and dystopia canthorum as major features. Diagnosed clinically using a Consortium criteria, this is one of the differential diagnoses when presented with a patient with bilateral blue eyes. There have been reports of this disorder in Asia but there are no known published articles or cases from the Philippines. Conclusion: This is the first reported case of Waardenburg Syndrome in the country. This case presented with an atypical combination of bilateral blue eyes and heterochromic fundi in a young Asian girl.  

Waardenburg syndrome blue iris Pale blue eyes heterochromic iris heterochromic fundi PAX gene dystopia canthorum hearing loss

Cited by 2

A Rare Case of Waardenburg-Shah Syndrome without Family History

Aryani Atiyatul Amra, Fithria Aldy, Barii Hafidh Pramono · Open Access Macedonian Journal of Medical Sciences · 2021

Genetic Eye Research in the Philippines

Patrick R. Ching, Edward Ryan A. Collantes, Michelle D. Lingao · Essentials in Ophthalmology · 2018

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