| Literature DB >> 3058052 |
C de Sousa1, T Clark, A Bradshaw.
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.Entities:
Mesh:
Year: 1988 PMID: 3058052 PMCID: PMC1590207 DOI: 10.1136/adc.63.10_spec_no.1168
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791