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Parabiotic twin syndrome with topical isocortical disruption and gastroschisis.

作者信息

Barth P G, van der Harten J J

出版信息

Acta Neuropathol. 1985;67(3-4):345-9. doi: 10.1007/BF00687825.

DOI:10.1007/BF00687825
PMID:3901653
Abstract

A case of parabiotic twin pregnancy is described with early fetal co-twin loss and topical isocortical disruption and gastroschisis in the surviving twin. We conclude from this case that early fetal parabiotic twin syndrome (before 16 weeks of gestational age) may cause microgyria and neuronal heterotopia. The cerebral and extracranial findings can be explained as the result of multiple vascular obstructions. Whereas most cases of parabiotic twin syndrome with brain damage involve cystic necrosis, focal hypoplasia with disrupted development in the affected part has been found in the present case. The probable reason in discussed. The roentgenographic analysis of the dead twin fetus is consistent with the period of 13-16 weeks as the likely period in which microgyria and neuronal heterotopia originated in the surviving twin. The present case constitutes one of the rare instances in which neuronal migration disturbance in the human could be dated reliably.

摘要

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本文引用的文献

1
Organ Abnormalities in a Human Parabiotic Syndrome.人类联体生活综合征中的器官异常
Am J Pathol. 1965 May;46(5):829-42.
2
Weights of organs of fetuses and infants.胎儿和婴儿器官的重量。
Arch Pathol. 1962 Sep;74:244-50.
3
Pathogenesis of four-layered microgyric cortex in man.人类四层微小脑回皮质的发病机制。
Acta Neuropathol Commun. 2014 Jul 22;2:80. doi: 10.1186/s40478-014-0080-3.
4
Gastroschisis, destructive brain lesions, and placental infarction in the second trimester suggest a vascular pathogenesis.孕中期出现腹裂、脑破坏性病变和胎盘梗死提示存在血管发病机制。
Pediatr Dev Pathol. 2013 Sep-Oct;16(5):391-6. doi: 10.2350/13-03-1316-CR.1. Epub 2013 Jul 30.
5
Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI.室管膜下结节性异位的位置与 MRI 上的畸形表型有关。
AJNR Am J Neuroradiol. 2013 Apr;34(4):877-83. doi: 10.3174/ajnr.A3312. Epub 2012 Oct 11.
6
Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria.编码紧密连接蛋白闭合蛋白的基因突变导致带型钙化,伴脑回简单化和脑回多小脑回。
Am J Hum Genet. 2010 Sep 10;87(3):354-64. doi: 10.1016/j.ajhg.2010.07.012. Epub 2010 Aug 19.
7
Cervical and intracranial arterial anomalies in 70 patients with PHACE syndrome.70 例 PHACE 综合征患者的颈内动脉和颅内动脉异常。
AJNR Am J Neuroradiol. 2010 Nov;31(10):1980-6. doi: 10.3174/ajnr.A2206. Epub 2010 Aug 12.
8
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.一致的染色体异常确定了1p36.3、2p16.1 - p23.1、4q21.21 - q22.1、6q26 - q27和21q2区域的新型多小脑回位点。
Am J Med Genet A. 2008 Jul 1;146A(13):1637-54. doi: 10.1002/ajmg.a.32293.
9
Magnetic resonance imaging of the fetal brain and spine: an increasingly important tool in prenatal diagnosis: part 2.胎儿脑与脊柱的磁共振成像:产前诊断中日益重要的工具:第2部分
AJNR Am J Neuroradiol. 2006 Oct;27(9):1807-14.
10
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems.KIAA1279基因的纯合无义突变与中枢和肠道神经系统畸形有关。
Am J Hum Genet. 2005 Jul;77(1):120-6. doi: 10.1086/431244. Epub 2005 May 9.
Acta Neuropathol. 1982;57(2-3):93-8. doi: 10.1007/BF00685375.
4
Cerebral, renal and splenic lesions due to fetal anoxia and their relationship to malformations.
Dev Med Child Neurol. 1982 Aug;24(4):510-8. doi: 10.1111/j.1469-8749.1982.tb13658.x.
5
Errors of morphogenesis: concepts and terms. Recommendations of an international working group.形态发生错误:概念与术语。一个国际工作组的建议
J Pediatr. 1982 Jan;100(1):160-5. doi: 10.1016/s0022-3476(82)80261-8.
6
Feto-fetal transfusion syndrome.胎儿-胎儿输血综合征
Arch Dis Child. 1982 Oct;57(10):781-3. doi: 10.1136/adc.57.10.781.
7
Congenital hydranencephaly/porencephaly due to vascular disruption in monozygotic twins.单卵双胞胎因血管破坏导致的先天性积水性无脑畸形/孔洞脑畸形。
Pediatrics. 1984 Apr;73(4):467-9.
8
Estimation of gestational age from measurements of fetal long bones.
J Ultrasound Med. 1984 Feb;3(2):75-9. doi: 10.7863/jum.1984.3.2.75.
9
The developmental pathogenesis of structural defects: the contribution of monozygotic twins.
Semin Perinatol. 1983 Oct;7(4):239-43.
10
The vascular pathogenesis of gastroschisis: intrauterine interruption of the omphalomesenteric artery.腹裂的血管发病机制:脐肠系膜动脉的宫内中断。
J Pediatr. 1981 Feb;98(2):228-31. doi: 10.1016/s0022-3476(81)80640-3.