- Three Cases of Waardenburg Syndrome Type 2 in a Korean Family
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Choi JH, Moon SK, Lee KH, Lew HM, Chang YH
- KMID: 754386
- Korean J Ophthalmol.
- 2004 Dec;18(2):185-189.
- doi: 10.3341/kjo.2004.18.2.185
Waardenburg syndrome (WS) is a rare, autosomal dominant disorder characterized by sensorineural hearing loss, pigmentary disturbances of the skin, hair, and iris, and other developmental defects such as lateral displacement... -
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