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Pierre Robin序列中大型腭裂的手术治疗:一例病例报告及文献综述

Surgical management of a large cleft palate in a Pierre Robin sequence: A case report and review of literature.

作者信息

Andrews Sherry, Sam Mathew, Krishnan Ramesh, Ramesh Maya, Kunjappan Shiji M

机构信息

Department of Oral and Maxillofacial Surgery, Armed Forces Hospital Southern Region, Kingdom of Saudi Arabia.

Department of Pedodontics, Vinayaka Missions Sankarachariyar Dental College, Salem, Tamil Nadu, India.

出版信息

J Pharm Bioallied Sci. 2015 Aug;7(Suppl 2):S718-20. doi: 10.4103/0975-7406.163498.

DOI:10.4103/0975-7406.163498
PMID:26538951
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4606693/
Abstract

Pierre Robin syndrome or Pierre Robin sequence (PRS) is a congenital etiologically heterogeneous condition presenting with various malformations. Here we are reporting the surgical management of an 18-month-old female baby who was referred from Department of Pediatrics with a complaint of a large cleft palate. She was taken up for palatoplasty with consent for elective tracheostomy. After genetic evaluation, the authors conclude that the presented case was a PRS in isolation with mild cardiac anomalies and an inferiorly placed hypoplastic epiglottis. Patient should be followed up and growth modifications of the jaws should be done.

摘要

皮埃尔·罗宾综合征或皮埃尔·罗宾序列征(PRS)是一种病因异质性的先天性疾病,伴有多种畸形。在此,我们报告一名18个月大女婴的手术治疗情况,该女婴由儿科转诊而来,主诉为巨大腭裂。她在获得择期气管切开术同意后接受了腭裂修复术。经过基因评估,作者得出结论,该病例为孤立性PRS,伴有轻度心脏异常和低位发育不全的会厌。应对患者进行随访,并对颌骨进行生长改良。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/99ac16e58413/JPBS-7-718-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/06d4e7ba88d3/JPBS-7-718-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/40d46cee9403/JPBS-7-718-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/76f0252c0033/JPBS-7-718-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/99ac16e58413/JPBS-7-718-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/06d4e7ba88d3/JPBS-7-718-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/40d46cee9403/JPBS-7-718-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/76f0252c0033/JPBS-7-718-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e9/4606693/99ac16e58413/JPBS-7-718-g005.jpg

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引用本文的文献

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Open Med (Wars). 2020 Sep 30;15(1):915-920. doi: 10.1515/med-2020-0231. eCollection 2020.
2
Identical twins with Pierre Robin syndrome; unusual encounter.患有皮埃尔·罗宾综合征的同卵双胞胎;罕见病例
Electron Physician. 2017 May 25;9(5):4296-4299. doi: 10.19082/4296. eCollection 2017 May.

本文引用的文献

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Mandibular distraction in neonates: indications, technique, results.新生儿下颌骨牵引:适应证、技术、结果。
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Cleft palate repair and variations.腭裂修复及变异
Indian J Plast Surg. 2009 Oct;42 Suppl(Suppl):S102-9. doi: 10.4103/0970-0358.57197.
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Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.与皮埃尔·罗宾序列相关的SOX9两侧高度保守的非编码元件。
Nat Genet. 2009 Mar;41(3):359-64. doi: 10.1038/ng.329. Epub 2009 Feb 22.
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Diagnosis and treatment of the Pierre Robin sequence: results of a retrospective clinical study and review of the literature.皮埃尔·罗宾序列征的诊断与治疗:一项回顾性临床研究结果及文献综述
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Congenital heart disease in the Pierre Robin syndrome.皮埃尔·罗宾综合征中的先天性心脏病。
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Incidence of the Robin Anomalad (Pierre Robin syndrome).罗宾序列征(皮埃尔·罗宾综合征)的发病率。
Br J Plast Surg. 1983 Oct;36(4):434-7. doi: 10.1016/0007-1226(83)90123-6.
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Anomalies associated with cleft lip, cleft palate, or both.与唇裂、腭裂或两者相关的异常情况。
Am J Med Genet. 1985 Apr;20(4):585-95. doi: 10.1002/ajmg.1320200404.