Archives of Disease in Childhood · 1988 · 52 citations · 5 references
MedicineObstetricsMaternal-fetal MedicinePrenatal DiagnosisBleeding DisordersCoagulation AbnormalitiesCoagulation DisordersCoagulation Factor DeficienciesCongenital DisordersHemostatic DisordersCongenital Bleeding DisordersFactor X MutationFactor X PhysiologyHereditary Factor X DeficiencyInherited Coagulation Factor DeficienciesReplacementSubdural Hemorrhage
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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Factor V deficiency and antenatal intraventricular haemorrhage.
Andrew Whitelaw, Morgan Haines, W Bolsover et al. · Archives of Disease in Childhood · 1984 · 45 citations · Full text
Replacement therapy for congenital Factor X deficiency
Robert Knight, CS Barr, Barbara M. Alving · Transfusion · 1985 · 40 citations
Medicine, Hematology, Surgery +17
Factor X deficiency in the neonatal period.
Samuel J. Machin, Mark Winter, S C Davies et al. · Archives of Disease in Childhood · 1980 · 28 citations · Full text
Medicine, Hematology, Pediatrics +17
[A new congenital coagulation defect; Stuart factor defect].
F Bachmann, F Duckert, P Flückiger et al. · PubMed · 1958 · 10 citations
Medicine, Genetics, Pediatrics +10