右半软腭完全缺失--病例报告

Pub Date : 2024-05-10 DOI:10.1055/s-0044-1786366
Ishan Agnihotri, Bibhuti Bhusan Nayak
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引用次数: 0

摘要

软腭缺失是一种极为罕见的疾病,通常与其他先天性畸形(如纳格综合征、特雷撤-科林斯综合征和多发性先天性畸形)同时出现。文献中仅报道过少数孤立的半侧软腭完全缺失的病例。尽管查阅了大量文献,但这样的病例几乎闻所未闻。我们为您介绍的病例符合上述所有条件。我们介绍的这例右半软腭发育不全病例采用了我们的技术进行治疗。
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Complete Agenesis of Right Half of Soft Palate—A Case Report
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.
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