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软腭右半侧完全缺如——病例报告

Complete Agenesis of Right Half of Soft Palate-A Case Report.

作者信息

Agnihotri Ishan, Nayak Bibhuti Bhusan

机构信息

Department of Plastic & Reconstructive Surgery, SCB Medical College, Cuttack, Odisha, India.

出版信息

Indian J Plast Surg. 2024 May 10;57(5):404-407. doi: 10.1055/s-0044-1786366. eCollection 2024 Oct.

Abstract

Agenesis of soft palate is an extremely rare occurrence and is usually seen in conjunction with other congenital anomalies like Nager syndrome, Treacher Collins syndrome, and multiple congenital anomalies. Only a handful of isolated complete agenesis of one half of the soft palate has been reported in literature. Despite extensive literature review, incidence of such a case is practically unheard of. We present to you a case checking all the above boxes. We present this case of agenesis of right half of soft palate that was managed by our technique.

摘要

软腭发育不全极为罕见,通常与其他先天性异常如纳格尔综合征、特雷彻·柯林斯综合征以及多种先天性异常同时出现。文献中仅报道过少数几例孤立的软腭一侧完全发育不全的病例。尽管进行了广泛的文献检索,但这种病例的发生率实际上闻所未闻。我们在此向您呈现一个符合上述所有情况的病例。我们展示这例右侧软腭发育不全的病例,该病例采用我们的技术进行了治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/1133701b33fd/10-1055-s-0044-1786366-i2412568-1.jpg

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