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本文引用的文献

1
Diagnosing arthrogryposis multiplex congenita: a review.先天性多发性关节挛缩症的诊断:综述
ISRN Obstet Gynecol. 2012;2012:264918. doi: 10.5402/2012/264918. Epub 2012 Sep 23.
2
Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review.胎儿运动障碍畸形序列和多翼畸形综合征伴神经肌肉接头疾病的产前诊断和遗传学分析:综述。
Taiwan J Obstet Gynecol. 2012 Mar;51(1):12-7. doi: 10.1016/j.tjog.2012.01.004.
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Arthrogryposis multiplex congenita and Pena-Shokeir phenotype: challenge of prenatal diagnosis--report of 21 cases, antenatal findings and review.先天性多发性关节挛缩症和 Pena-Shokeir 表型:产前诊断的挑战——21 例病例的产前发现和回顾。
Fetal Diagn Ther. 2011;30(4):289-98. doi: 10.1159/000331401. Epub 2011 Dec 8.
4
Antenatal ultrasound and MRI findings of Pena-Shokeir syndrome.产前超声和磁共振成像在佩纳-绍克尔综合征的表现。
Arch Gynecol Obstet. 2011 Mar;283 Suppl 1:27-9. doi: 10.1007/s00404-010-1703-y. Epub 2010 Oct 12.
5
Pena-Shokeir phenotype (fetal akinesia deformation sequence) revisited.再探佩纳-绍凯尔综合征(胎儿运动减少性变形序列征)
Birth Defects Res A Clin Mol Teratol. 2009 Aug;85(8):677-94. doi: 10.1002/bdra.20611.
6
Pena-Shokeir phenotype with variable onset in three consecutive pregnancies.三例连续妊娠中出现不同发病时间的佩纳-绍凯尔综合征表型
Ultrasound Obstet Gynecol. 2001 Feb;17(2):163-5. doi: 10.1046/j.1469-0705.2001.00246.x.
7
Prenatal ultrasound of regional akinesia with Pena-Shokier phenotype.具有佩纳-绍基尔表型的局部运动不能的产前超声检查。
Prenat Diagn. 2000 May;20(5):422-5. doi: 10.1002/(sici)1097-0223(200005)20:5<422::aid-pd838>3.0.co;2-g.
8
Ultrasound diagnosis of the Pena Shokeir phenotype at 14 weeks of pregnancy.妊娠14周时佩纳-绍凯尔表型的超声诊断。
Prenat Diagn. 1995 Aug;15(8):762-4. doi: 10.1002/pd.1970150813.
9
Arthrogryposis-like signs in trisomy 18.18三体综合征中的关节挛缩样体征。
Hum Genet. 1981;57(2):145-7. doi: 10.1007/BF00282011.
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Fetal akinesia deformation sequence: an animal model.胎儿运动不能变形序列征:一种动物模型。
Pediatrics. 1983 Dec;72(6):857-63.

1例佩纳-绍凯尔综合征(Pena-Shokeir phenotype)患者的产前超声检查结果及磁共振成像

Antenatal ultrasonography findings and magnetic resonance imaging in a case of Pena-Shokeir phenotype.

作者信息

Tomai Xuan-Hong, Jasmine Thanh-Xuan, Phan Thanh-Hai

机构信息

Department of Obstetrics and Gynecology, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.

Medic Medical Center, Ho Chi Minh City, Vietnam.

出版信息

Ultrasound. 2017 May;25(2):115-119. doi: 10.1177/1742271X16688235. Epub 2017 Jan 10.

DOI:10.1177/1742271X16688235
PMID:28567106
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5438052/
Abstract

Pena-Shokeir phenotype is a lethal anomaly characterized by neurogenic arthrogryposis, craniofacial anomalies, and pulmonary hypoplasia. This syndrome should be distinguished from trisomy 18 and arthrogryposis multiplex congenita for better counseling and establishing fetal prognosis. We present the case of a pregnant woman diagnosed with a Pena-Shokeir phenotype affected fetus at 24 weeks of gestation. Prenatal ultrasonography and fetal magnetic resonance imaging detected persistent hyperextension of the lumbar spine, micrognathia, absent septum pellucidum, and all characteristic features of Pena-Shokeir phenotype. Karyotyping was performed to exclude fetal chromosomal anomalies. Antenatal ultrasonography is an essential tool in the diagnosis of Pena-Shokeir phenotype while fetal magnetic resonance imaging is necessary to identify any associated anomalies of central nervous system.

摘要

佩纳-绍凯尔综合征是一种致死性畸形,其特征为神经源性关节挛缩、颅面畸形和肺发育不全。为了更好地进行咨询和确定胎儿预后,应将该综合征与18三体综合征和先天性多发性关节挛缩症相区分。我们报告一例在妊娠24周时被诊断为患有佩纳-绍凯尔综合征胎儿的孕妇病例。产前超声检查和胎儿磁共振成像检测到腰椎持续过度伸展、小颌畸形、透明隔缺如以及佩纳-绍凯尔综合征的所有特征性表现。进行了染色体核型分析以排除胎儿染色体异常。产前超声检查是诊断佩纳-绍凯尔综合征的重要工具,而胎儿磁共振成像对于识别任何中枢神经系统相关异常是必要的。