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先天性因子X缺乏症产前诊断为硬膜下出血。

Antenatally diagnosed subdural haemorrhage in congenital factor X deficiency.

作者信息

de Sousa C, Clark T, Bradshaw A

机构信息

Department of Paediatrics, Hammersmith Hospital, London.

出版信息

Arch Dis Child. 1988 Oct;63(10 Spec No):1168-70. doi: 10.1136/adc.63.10_spec_no.1168.

DOI:10.1136/adc.63.10_spec_no.1168
PMID:3058052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1590207/
Abstract

The presence of a subdural haemorrhage was observed in a fetus during antenatal ultrasound examination. The infant was found to be a homozygote for factor X deficiency. Prompt recognition permitted replacement treatment from an early stage. Inherited coagulation disorders should be suspected when intracranial haemorrhage is detected antenatally.

摘要

产前超声检查时在一名胎儿中观察到硬膜下出血。发现该婴儿为X因子缺乏的纯合子。及时识别使得能够从早期就开始进行替代治疗。产前检测到颅内出血时，应怀疑存在遗传性凝血障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c737/1590207/012d81fec61b/archdisch00903-0057-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c737/1590207/b1b353bfd6d5/archdisch00903-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c737/1590207/012d81fec61b/archdisch00903-0057-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c737/1590207/b1b353bfd6d5/archdisch00903-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c737/1590207/012d81fec61b/archdisch00903-0057-a.jpg

相似文献

1
Antenatally diagnosed subdural haemorrhage in congenital factor X deficiency.先天性因子X缺乏症产前诊断为硬膜下出血。
Arch Dis Child. 1988 Oct;63(10 Spec No):1168-70. doi: 10.1136/adc.63.10_spec_no.1168.
2
[A disorder in the coagulation mechanism as a possible cause for the development of an antenatal intracranial hemorrhage].
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引用本文的文献

1
Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency.遗传性因子 X 缺乏症患者严重出血发作的发生和处理。
Haemophilia. 2021 Jul;27(4):531-543. doi: 10.1111/hae.14223. Epub 2021 May 22.

本文引用的文献

1
[A new congenital coagulation defect; Stuart factor defect].[一种新的先天性凝血缺陷；斯图尔特因子缺陷]
Thromb Diath Haemorrh. 1958 Apr 15;1(1):87-92.
2
Factor X deficiency in the neonatal period.
Arch Dis Child. 1980 May;55(5):406-8. doi: 10.1136/adc.55.5.406.
3
Unexplained intracranial haemorrhage in utero: the battered fetus?子宫内原因不明的颅内出血：受虐胎儿？
Aust N Z J Obstet Gynaecol. 1984 Feb;24(1):17-22. doi: 10.1111/j.1479-828x.1984.tb03315.x.
4
Factor V deficiency and antenatal intraventricular haemorrhage.凝血因子V缺乏与产前脑室内出血。
Arch Dis Child. 1984 Oct;59(10):997-9. doi: 10.1136/adc.59.10.997.
5
Inherited factor X deficiency: presentation of a case with etiologic and treatment considerations.遗传性因子X缺乏症：1例病例的临床表现及病因和治疗考量
Oral Surg Oral Med Oral Pathol. 1983 Nov;56(5):461-6. doi: 10.1016/0030-4220(83)90088-9.
6
Replacement therapy for congenital Factor X deficiency.
Transfusion. 1985 Jan-Feb;25(1):78-80. doi: 10.1046/j.1537-2995.1985.25185116511.x.