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.
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。
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