Beck Anita E, Hudgins Louanne, Hoyme H Eugene
Department of Genetics, Stanford University School of Medicine, Stanford, California 94305-5323, USA.
Am J Med Genet A. 2005 May 1;134(4):359-62. doi: 10.1002/ajmg.a.30638.
The oculo-auriculo-vertebral (OAV) spectrum is an etiologically heterogeneous condition classically consisting of microtia, hemifacial microsomia, epibulbar dermoids, and vertebral anomalies. Other eye findings described in OAV include upper eyelid colobomas, ptosis, and varying degrees of microphthalmia or even anophthalmia. Iris and/or retinal colobomas have rarely been reported. We describe two familial cases of apparent OAV with ocular colobomas. We postulate that iris and/or retinal colobomas associated with OAV may represent a subgroup within the OAV spectrum with autosomal dominant inheritance, as in the families described herein. Since microtia can result from aberrant migration of neural crest cells into the first and second branchial arches during early embryonic development, and concomitant deficient neural crest migration into the developing eye can lead to ocular coloboma and or iris heterochromia, it may be that the altered gene or genes in our familial cases are involved with regulation of neural crest development.
眼-耳-脊椎(OAV)谱系是一种病因学上异质性的疾病,典型表现包括小耳畸形、半侧颜面短小、眼球表面皮样囊肿和脊椎异常。OAV中描述的其他眼部表现包括上睑裂缺、上睑下垂以及不同程度的小眼畸形甚至无眼畸形。虹膜和/或视网膜裂缺很少有报道。我们描述了两例伴有眼部裂缺的疑似OAV家族病例。我们推测,与OAV相关的虹膜和/或视网膜裂缺可能代表OAV谱系中具有常染色体显性遗传的一个亚组,如本文所述的家族病例。由于小耳畸形可能是由于神经嵴细胞在胚胎早期发育过程中异常迁移至第一和第二鳃弓,同时神经嵴向发育中的眼睛迁移不足可导致眼部裂缺和/或虹膜异色,因此我们家族病例中改变的一个或多个基因可能参与神经嵴发育的调控。