Ozturk Ozcan, Tokmak Abdurrahman, Demirci Levent, Silan Fatma, Guclu Ender
Department of Otorhinolaryngology, Duzce Medical Faculty, 81010 Duzce, Turkey.
Int J Pediatr Otorhinolaryngol. 2005 Nov;69(11):1575-8. doi: 10.1016/j.ijporl.2005.04.013. Epub 2005 Jun 4.
We report an 8-year-old child with branchio-oculo-facial syndrome. He showed atresia of external ear, preauricular pit, maxillar and mandibular hypoplasia, mild ptosis on the left side, lacrimal duct obstruction, unilateral branchial cyst, hypertrichosis of the neck, left foot showed mild syndactily of fourth and fifth toes and dental abnormalities. His mother had pseudocleft of the lip which led to the diagnosis. The importance of serial observations in patients with rare genetic disorders is emphasized.
我们报告了一名患有鳃-眼-面综合征的8岁儿童。他表现出外耳道闭锁、耳前瘘管、上颌骨和下颌骨发育不全、左侧轻度上睑下垂、泪道阻塞、单侧鳃裂囊肿、颈部多毛症、左脚第四和第五趾轻度并指以及牙齿异常。他的母亲有唇裂假畸形,这有助于做出诊断。强调了对罕见遗传疾病患者进行系列观察的重要性。