A Case of Waardenburg`s Syndrome
Journal of the Korean Ophthalmological Society
; : 2247-2250, 1997.
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.
Key words
Full text:
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Index:
WPRIM
Main subject:
Genetic Diseases, Inborn
Limits:
Adult
/
Female
/
Humans
Language:
Ko
Journal:
Journal of the Korean Ophthalmological Society
Year:
1997
Type:
Article