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小耳畸形的胚胎学与流行病学

Embryology and epidemiology of microtia.

作者信息

Klockars Tuomas, Rautio Jorma

机构信息

Department of Otorhinolaryngology, Helsinki University Central Hospital, Helsinki, Finland.

出版信息

Facial Plast Surg. 2009 Aug;25(3):145-8. doi: 10.1055/s-0029-1239444. Epub 2009 Oct 6.

Abstract

The auricle derives from six hillocks arising from the first and second branchial arches. Different hillocks give rise to different parts of the pinna. In the course of embryonic development, the auricle migrates postero-cranially as the mandible enlarges. Auricular malformations, such as microtia, are thought to be related to cell death of the first and second arch derivatives. The prevalence and characteristics of microtia vary in different populations. The prevalence ranges from 0.83 to 17.4 per 10,000. Microtia is more common in males, and right-sided dominance varies from 57 to 67%. The prevalence of aural atresia or stenosis varies from 55 to 93%. Microtia has been associated with numerous risk factors including race and gender. Genetic factors are likely to have an effect at least in some patients with microtia.

摘要

耳廓起源于第一和第二鳃弓上出现的六个小丘。不同的小丘发育形成耳廓的不同部分。在胚胎发育过程中,随着下颌骨的增大,耳廓向后颅侧迁移。耳廓畸形,如小耳症,被认为与第一和第二鳃弓衍生物的细胞死亡有关。小耳症的患病率和特征在不同人群中有所不同。患病率为每10000人中有0.83至17.4例。小耳症在男性中更为常见,右侧优势率在57%至67%之间。耳道闭锁或狭窄的患病率在55%至93%之间。小耳症与多种风险因素有关,包括种族和性别。遗传因素可能至少在一些小耳症患者中起作用。

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