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首页> 外文期刊>Journal of International Medical Research >Branchial cleft fistula to branchio-oto-renal syndrome: A case report and literature review
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Branchial cleft fistula to branchio-oto-renal syndrome: A case report and literature review

机译:鳃裂瘘到枝耳综合征:案例报告和文献综述

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摘要

Branchial cleft abnormality is a common congenital neck malformation in children, which is caused by the abnormal development of the gill sac or gill groove. It is mainly manifested as a cyst in the sinus tract and fistula in the neck, as well as branchio-oto-renal syndrome (BORS). As a rare autosomal dominant genetic disease, the typical manifestations of BORS are hearing loss, abnormal branchial cleft development and renal dysplasia. In this paper, a patient was admitted to the hospital for bilateral branchial cleft fistulas combined with bilateral anterior auricular fistulas, auricular appendix, auricle dysplasia, external auditory canal stenosis, and hearing loss. The patient was diagnosed with BORS, and underwent fistulectomy of the neck and anterior ear, external auditory canal formation, and tympanoplasty. The aim of this report is to strengthen clinicians’ understanding of BORS and reduce the rate of clinical missed diagnosis through our case report and literature review.
机译:鳃裂异常是儿童中共同的先天性颈部畸形,这是由鳃囊或鳃槽的异常发育引起的。它主要表现为鼻窦和颈部瘘管的囊肿,以及骨质 - 耳肾综合征(BORS)。作为一种稀有的常染色体显性遗传疾病,婴儿床的典型表现是听力丧失,鳃裂开的异常发育和肾功能不良。本文患有患者的双侧鳃裂式瘘管,联合双侧前耳瘘,耳廓附录,耳廓发育不良,外观渠道狭窄和听力损失。患者被诊断为母羊,并接受颈部和前耳的瘘管切除术,外耳,外耳形成和鼓膜成形术。本报告的目的是通过案例报告和文献审查,加强临床医生对母鸡的理解,并降低临床未错过诊断速度。

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