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Hydranencephaly; clinical diagnosis; presentation of 7 cases.

作者信息

HAMBY W B, KRAUSS R F, BESWICK W F

出版信息

Pediatrics. 1950 Sep;6(3):371-83.

PMID:14780790
Abstract
摘要

相似文献

1
Hydranencephaly; clinical diagnosis; presentation of 7 cases.积水性无脑畸形;临床诊断;7例病例报告
Pediatrics. 1950 Sep;6(3):371-83.
2
Looking at the missing brain: hydranencephaly case series and literature review.关注缺失的大脑:无脑畸形病例系列和文献复习。
Pediatr Neurol. 2013 Feb;48(2):152-8. doi: 10.1016/j.pediatrneurol.2012.10.009.
3
Diagnostic image evaluation of hydranencephaly and pictorially similar entities, with emphasis on computed tomography.积水性无脑畸形及影像类似病变的诊断性影像评估,重点为计算机断层扫描
Radiology. 1980 Oct;137(1 Pt 1):81-91. doi: 10.1148/radiology.137.1.7422865.
4
Hydranencephaly in an infant with vascular malformations.患有血管畸形的婴儿的积水性无脑畸形
Am J Med Genet. 2001 Dec 15;104(4):295-8.
5
Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine.一名患有FLVCR2突变且产前接触过可卡因的新生儿出现积水性无脑畸形。
Birth Defects Res A Clin Mol Teratol. 2015 Jan;103(1):45-50. doi: 10.1002/bdra.23288. Epub 2014 Jul 30.
6
Hydranencephaly associated with interruption of bilateral internal carotid arteries.双侧颈内动脉中断相关的积水性无脑畸形。
Pediatr Neonatol. 2008 Apr;49(2):43-7. doi: 10.1016/S1875-9572(08)60011-X.
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
Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler type.两名患有早发性胎儿运动减少变形序列和积水性无脑畸形的兄弟姐妹:福勒型积水性无脑畸形常染色体隐性遗传的进一步证据。
Am J Med Genet. 2002 Feb 15;108(1):41-4.
9
[Pathology of hydranencephaly].[积水性无脑畸形的病理学]
Arkh Patol. 1983;45(4):16-9.
10
Hydranencephaly and maximal hydrocephalus: usefulness of electrophysiological studies for their differentiation.积水性无脑畸形与巨大脑积水:电生理研究对二者鉴别的作用
J Child Neurol. 1989 Apr;4(2):114-7. doi: 10.1177/088307388900400207.

引用本文的文献

1
The genetic etiologies of bilateral renal agenesis.双侧肾发育不全的遗传病因。
Prenat Diagn. 2024 Feb;44(2):205-221. doi: 10.1002/pd.6516. Epub 2024 Jan 5.
2
An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia.一个阿米什人变异种导致 CEP55 破坏,引起无脑畸形和肾发育不良。
Eur J Hum Genet. 2019 Apr;27(4):657-662. doi: 10.1038/s41431-018-0306-0. Epub 2019 Jan 8.
3
A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis.
CEP55基因中的截短突变可能是MARCH的病因,MARCH是一种影响神经元有丝分裂的新型综合征。
J Med Genet. 2017 Jul;54(7):490-501. doi: 10.1136/jmedgenet-2016-104296. Epub 2017 Mar 6.
4
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles.积水性无脑畸形:脑脊液替代了大脑皮质。
Ital J Pediatr. 2014 Oct 18;40:79. doi: 10.1186/s13052-014-0079-1.
5
Hydranencephaly and allied disorders: a study of cerebral defect in Chinese children.积水性无脑畸形及相关病症:中国儿童脑缺陷研究
Arch Dis Child. 1959 Jun;34(175):231-46. doi: 10.1136/adc.34.175.231.
6
The value of transillumination of the skull in neurological examination of neonates and infants.颅骨透照在新生儿和婴儿神经学检查中的价值。
Acta Neurochir (Wien). 1961;10:75-91. doi: 10.1007/BF01435727.
7
Hydranencephaly (hydrencephaly).积水性无脑畸形(脑积水)。
Arch Dis Child. 1958 Jun;33(169):235-45. doi: 10.1136/adc.33.169.235.
8
Hydranencephaly.积水性无脑畸形
Arch Dis Child. 1956 Jun;31(157):195-7. doi: 10.1136/adc.31.157.195.
9
[Comparative study of prenatal and perinatal circulatory encephalopathies (hydranencephalies, porencephalies and cystic encephalomalacias of the white matter)].产前和围产期循环性脑病(积水性无脑畸形、孔洞脑畸形和白质囊性脑软化)的比较研究
Acta Neuropathol. 1967 Aug 2;9(1):79-98. doi: 10.1007/BF00688160.
10
[Hydranencephaly versus spelencephaly--a report of two cases (author's transl)].积水性无脑畸形与孔洞脑畸形——两例报告(作者译)
Arch Psychiatr Nervenkr (1970). 1977 Sep 14;224(1):27-38. doi: 10.1007/BF00342082.