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A Case of Waardenburg`s Syndrome
Article in Ko | WPRIM | ID: wpr-188428
Responsible library: WPRO
ABSTRACT
Waardenburg`s syndrome is a rare hereditary disease, which is characterized by dystopia canthorum, hypochromic heterochromic iridum, sensorineural deafness,high and broad nasal bridge, white forelock and premature graying. We present a case of 27 year old woman with Waardenburg`s syndrome. She has characteristic features such as dystopia canthorum, broad and high nasal bridge, confluent eyebrow(synophrys), hypochromic heterochromic iridum, depigmented fundus and premature graying.
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Full text: 1 Index: WPRIM Main subject: Genetic Diseases, Inborn Limits: Adult / Female / Humans Language: Ko Journal: Journal of the Korean Ophthalmological Society Year: 1997 Type: Article
Full text: 1 Index: WPRIM Main subject: Genetic Diseases, Inborn Limits: Adult / Female / Humans Language: Ko Journal: Journal of the Korean Ophthalmological Society Year: 1997 Type: Article