Homozygous Protein C Deficiency in a Newborn
- 1 February 1988
- journal article
- case report
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 45 (2) , 214-216
- https://doi.org/10.1001/archneur.1988.00520260102029
Abstract
• A rare case of homozygous protein C deficiency occurred in a newborn. The patient presented with purpura fulminans in the first few hours after birth and showed multiple hemorrhagic lesions on computed tomography of the brain at 5 days of age. Neurologic symptoms developed at two weeks and the patient died at 37 weeks. His protein C level was less than 5%. Autopsy revealed thrombosis of the dural sinuses, multiple cortical infarcts, intraparenchymal hemorrhages, and hydrocephalus. The pathologic findings are correlated with the neurologic deficits and previously documented cases are reviewed.Keywords
This publication has 4 references indexed in Scilit:
- The Regulation of Hemostasis: The Protein C SystemNew England Journal of Medicine, 1986
- Homozygous protein C deficiency combined with heterozygous dysplasminogenemia found in a 21-year-old thrombophilic maleThrombosis Research, 1985
- Hereditary Protein C DeficiencyPathophysiology of Haemostasis and Thrombosis, 1985
- Purpura Fulminans in a Newborn BabyArchives of Disease in Childhood, 1962