Nayak Chetan S, Isaacson Glenn
Department of Otolaryngology-Head and Neck Surgery, Temple University School of Medicine, Temple University Children's Medical Center, Philadelphia, Pennsylvania 19140, USA.
Ann Otol Rhinol Laryngol. 2003 Sep;112(9 Pt 1):817-20. doi: 10.1177/000348940311200913.
To clarify the multiracial occurrence of Waardenburg syndrome, we present a case series and literature review. A computerized review of the English-language literature was conducted to assess the distribution of reported occurrences of Waardenburg syndrome in populations around the world. We detail the clinical features of 2 family cohorts: one of Western European origin and the other from South Asia. A computerized literature review found sporadic cases of the syndrome in many ethnic groups, including Japanese, Taiwanese, and Middle Eastern families. The highest reported incidence is among Kenyan Africans. Waardenburg syndrome accounts for between 2% and 5% of cases of congenital deafness. It was first described in Northern European cohorts and is widely identified in fair-skinned populations. We hope to raise awareness of the worldwide distribution of this important cause of hearing loss.
为阐明瓦登伯革氏综合征在多种族人群中的发病情况,我们呈现了一个病例系列并进行了文献综述。我们对英文文献进行了计算机检索,以评估世界各地人群中报道的瓦登伯革氏综合征发病情况的分布。我们详细描述了两个家族队列的临床特征:一个是西欧血统,另一个来自南亚。计算机文献检索发现该综合征在许多种族群体中都有散发病例,包括日本、台湾以及中东家庭。报道发病率最高的是肯尼亚非洲人。瓦登伯革氏综合征占先天性耳聋病例的2%至5%。它最初在北欧队列中被描述,并且在白皮肤人群中被广泛识别。我们希望提高对这一导致听力损失的重要病因在全球分布情况的认识。