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A Case of Waardenburg`s Syndrome
Journal of the Korean Ophthalmological Society ; : 2247-2250, 1997.
Artigo em Coreano | WPRIM | ID: wpr-188428
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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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Doenças Genéticas Inatas Limite: Adulto / Feminino / Humanos Idioma: Coreano Revista: Journal of the Korean Ophthalmological Society Ano de publicação: 1997 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Doenças Genéticas Inatas Limite: Adulto / Feminino / Humanos Idioma: Coreano Revista: Journal of the Korean Ophthalmological Society Ano de publicação: 1997 Tipo de documento: Artigo