瓦登伯革氏症候群

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瓦登伯革氏症候群
分類系統及外部資源
ICD-10 E70.3 (ILDS E70.32)
ICD-9 270.2
DiseasesDB 14021 33475
MedlinePlus 001428
eMedicine ped/2422 derm/690
MeSH D014849

瓦登伯革氏症候群英语Waardenburg syndrome)是一種罕見的遺傳性疾病,首次發現於1951年。[1]常見病徵為不同程度的耳聾,兩眼眼距較寬,鼻根寬闊,少年白髮,及出現虹膜異色症,即兩眼皆為藍眼珠或兩眼一藍一正常。

參考文獻[编辑]

  1. ^ Waardenburg PJ. A New Syndrome Combining Developmental Anomalies of the Eyelids, Eyebrows and Noseroot with Pigmentary Anomalies of the Iris and Head Hair and with Congenital Deafness; Dystopia canthi medialis et punctorum lacrimalium lateroversa, Hyperplasia supercilii medialis et radicis nasi, Heterochromia iridum totalis sive partialis, Albinismus circumscriptus (leucismus, poliosis) et Surditas congenita (surdimutitas). Am. J. Hum. Genet. 1951.September, 3 (3): 195–253. PMC 1716407. PMID 14902764. 

外部連結[编辑]