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本文引用的文献

1
Are ultrasonography measurements of optic nerve sheath diameter an alternative to funduscopy in children with syndromic craniosynostosis?对于患有综合征性颅缝早闭的儿童,视神经鞘直径的超声测量能否替代眼底镜检查?
J Neurosurg Pediatr. 2011 Sep;8(3):329-34. doi: 10.3171/2011.6.PEDS10547.
2
Comparison of spring-mediated cranioplasty to minimally invasive strip craniectomy and barrel staving for early treatment of sagittal craniosynostosis.弹簧介导颅骨成形术与微创条带颅骨切除术及桶状劈开术治疗矢状缝早闭的比较
J Craniofac Surg. 2011 Jul;22(4):1225-9. doi: 10.1097/SCS.0b013e31821c0f10.
3
Does the incidence of traumatic brain injury in children increase after craniofrontal surgery?儿童颅额部手术后创伤性脑损伤的发生率会增加吗?
J Craniofac Surg. 2011 Jul;22(4):1284-6. doi: 10.1097/SCS.0b013e31821c6b2d.
4
Complex craniosynostosis.复杂颅缝早闭。
Plast Reconstr Surg. 2011 Oct;128(4):955-961. doi: 10.1097/PRS.0b013e3182268ca6.
5
Expansion of the posterior cranial vault using distraction osteogenesis.应用牵张成骨术扩大颅后窝。
Plast Reconstr Surg. 2011 Feb;127(2):792-801. doi: 10.1097/PRS.0b013e318200ab83.
6
Occipital expansion without osteotomies in Apert syndrome.Apert综合征中无需截骨的枕骨扩展术
Childs Nerv Syst. 2010 Nov;26(11):1543-8. doi: 10.1007/s00381-010-1144-8. Epub 2010 Apr 9.
7
The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndrome.TWIST1 确诊的 Saethre-Chotzen 综合征患者的自然病史。
Plast Reconstr Surg. 2009 Dec;124(6):2085-2095. doi: 10.1097/PRS.0b013e3181bf83ce.
8
Discussion. Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.讨论。TWIST1基因确诊的塞-乔二氏综合征患者颅内高压的再次手术治疗:一项15年的回顾性研究
Plast Reconstr Surg. 2009 Jun;123(6):1811-1812. doi: 10.1097/PRS.0b013e3181a3f213.
9
Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.TWIST1基因确诊的塞-乔二氏综合征患者颅内高压的再次手术治疗:一项15年的回顾性研究
Plast Reconstr Surg. 2009 Jun;123(6):1801-1810. doi: 10.1097/PRS.0b013e3181a3f391.
10
Pfeiffer syndrome: a treatment evaluation.法伊弗综合征:一项治疗评估。
Plast Reconstr Surg. 2009 May;123(5):1560-1569. doi: 10.1097/PRS.0b013e3181a2057e.

综合征型颅缝早闭。

Syndromic craniosynostosis.

机构信息

Department of Plastic Surgery, University of Texas Southwestern Medical Center, Dallas, Texas.

出版信息

Semin Plast Surg. 2012 May;26(2):64-75. doi: 10.1055/s-0032-1320064.

DOI:10.1055/s-0032-1320064
PMID:23633933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3424695/
Abstract

Although most cases of craniosynostosis are nonsyndromic, craniosynostosis is known to occur in conjunction with other anomalies in well-defined patterns that make up clinically recognized syndromes. Patients with syndromic craniosynostoses are much more complicated to care for, requiring a multidisciplinary approach to address all of their needs effectively. This review describes the most common craniosynostosis syndromes, their characteristic features and syndrome-specific functional issues, and new modalities utilized in their management. General principles including skull development, the risk of developing increased intracranial pressure in craniosynostosis syndromes, and techniques to measure intracranial pressure are discussed. Evolving techniques of the established operative management of craniosynostosis are discussed together with more recent techniques including spring cranioplasty and posterior cranial vault distraction osteogenesis.

摘要

虽然大多数颅缝早闭病例是非综合征性的,但颅缝早闭与其他异常情况同时发生,形成明确的模式,构成临床上公认的综合征。患有综合征性颅缝早闭的患者需要更复杂的护理,需要采用多学科方法来有效满足他们的所有需求。这篇综述描述了最常见的颅缝早闭综合征、它们的特征和综合征特异性功能问题,以及在其治疗中使用的新方法。讨论了一般原则,包括颅骨发育、颅缝早闭综合征中颅内压升高的风险以及测量颅内压的技术。讨论了已确立的颅缝早闭手术治疗的不断发展的技术,以及包括弹簧颅骨成形术和颅后穹窿牵引成骨术在内的较新技术。