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瓦登伯格氏症候群-病例報告

Waardenburg Syndrome - A Case Report

摘要


瓦登伯格氏症候群為一罕見疾病,患者臨床症狀常見為藍眼珠(虹膜異色症)、先天聽障、內眥外移等。本文案例為一患有此病的3歲男童,先天聽力障礙,由家長帶至門診主訴為發現有蛀牙且診所無法處理。經臨床檢查後發現,口內嚴重齲齒且先天聽力障礙行為難以合作,故在全身麻醉下進行全口重建。本文亦討論此症候群之臨床表徵、遺傳形式、分類及診斷。

並列摘要


Waardenburg Syndrome(WAS) is a rare multiple congenital anomaly syndrome. This syndrome is characterized by hete-rochromia iris, dystopia canthorum, white forelock, depigmentation of skin and congenital hearing impairment. This article presents a case of 3-year-old boy with Waardenburg Syndrome(WAS). Because of his multiple caries, hearing loss and uncooperative behavior, we treated his caries under general anesthesia. The clinical manifestations, mode of inheritance, diagnostic criteria and clinical classification of Waardenburg syndrome are also addressed.

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