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本文引用的文献

1
The face of Joubert syndrome: a study of dysmorphology and anthropometry.乔伯特综合征的面容:畸形学与人体测量学研究
Am J Med Genet A. 2007 Dec 15;143A(24):3235-42. doi: 10.1002/ajmg.a.32099.
2
Joubert syndrome (and related disorders) (OMIM 213300).乔伯特综合征(及相关疾病)(在线人类孟德尔遗传数据库编号213300)
Eur J Hum Genet. 2007 May;15(5):511-21. doi: 10.1038/sj.ejhg.5201648. Epub 2007 Mar 21.
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Prenatal diagnosis of episodic tachypnea in an infant with OFD VI.一名患有口面指综合征VI型婴儿的发作性呼吸急促的产前诊断。
Am J Med Genet A. 2006 Oct 1;140(19):2146-9. doi: 10.1002/ajmg.a.31406.
4
Molar tooth sign in fetal brain magnetic resonance imaging leading to the prenatal diagnosis of Joubert syndrome and related disorders.胎儿脑磁共振成像中的磨牙征导致Joubert综合征及相关疾病的产前诊断。
J Child Neurol. 2006 Apr;21(4):320-4. doi: 10.1177/08830738060210041001.
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Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRI.通过超声和磁共振成像对存在乔伯特综合征风险的妊娠进行产前诊断。
Prenat Diagn. 2005 Jun;25(6):442-7. doi: 10.1002/pd.1145.
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Prenatal sonographic findings in a case of Varadi-Papp syndrome.Varadi-Papp综合征一例的产前超声检查结果
Prenat Diagn. 2004 Dec 15;24(12):989-91. doi: 10.1002/pd.916.
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MRI of the fetal posterior fossa.胎儿后颅窝的磁共振成像
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8
Pre- and postnatal MR imaging of hypothalamic hamartomas associated with arachnoid cysts.与蛛网膜囊肿相关的下丘脑错构瘤的产前和产后磁共振成像
AJNR Am J Neuroradiol. 2004 Aug;25(7):1283-5.
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MR imaging and spectroscopic study of epileptogenic hypothalamic hamartomas: analysis of 72 cases.致痫性下丘脑错构瘤的磁共振成像及波谱研究:72例分析
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Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.中脑-后脑交界处的磨牙征:在多种不同综合征中的出现情况。
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口面指综合征VI型的产前和新生儿磁共振成像表现

Prenatal and neonatal MR imaging findings in oral-facial-digital syndrome type VI.

作者信息

Poretti A, Brehmer U, Scheer I, Bernet V, Boltshauser E

机构信息

Department of Pediatric Neurology, University Children's Hospital of Zurich, Zurich, Switzerland.

出版信息

AJNR Am J Neuroradiol. 2008 Jun;29(6):1090-1. doi: 10.3174/ajnr.A1038. Epub 2008 Mar 20.

DOI:10.3174/ajnr.A1038
PMID:18356465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8118817/
Abstract

We report prenatal and neonatal neuroimaging findings in a case of oral-facial-digital syndrome type VI (OFDS VI). Prenatal MR imaging at 29 weeks' gestation showed hypoplastic cerebellar vermis and hemispheres, the molar tooth sign, and a hypothalamic hamartoma. Neonatal MR imaging confirmed these findings. The neonate developed breathing abnormalities and exhibited frontal bossing, multiple bucco-alveolar frenula, and postaxial hexadactyly of both hands. If the molar tooth sign and a hypothalamic hamartoma are present, prenatal diagnosis of OFDS VI is possible.

摘要

我们报告了一例Ⅵ型口面指综合征(OFDS VI)的产前和新生儿神经影像学检查结果。妊娠29周时的产前磁共振成像显示小脑蚓部和半球发育不全、磨牙征以及下丘脑错构瘤。新生儿磁共振成像证实了这些发现。该新生儿出现呼吸异常,并表现出前额突出、多个颊牙槽系带以及双手轴后多指畸形。如果存在磨牙征和下丘脑错构瘤,则有可能在产前诊断OFDS VI。