Antenatally diagnosed subdural haemorrhage in congenital factor X deficiency

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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.

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APA

De Sousa, C., Clark, T., & Bradshaw, A. (1988). Antenatally diagnosed subdural haemorrhage in congenital factor X deficiency. Archives of Disease in Childhood, 63(10 SPEC NO.), 1168–1170. https://doi.org/10.1136/adc.63.10_Spec_No.1168

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