Homozygous protein C deficiency in a newborn. Clinicopathologic correlation

Arch Neurol. 1988 Feb;45(2):214-6. doi: 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.

Publication types

  • Case Reports

MeSH terms

  • Blood Coagulation Disorders / congenital
  • Blood Coagulation Disorders / etiology
  • Blood Coagulation Disorders / genetics
  • Brain / pathology*
  • Cerebral Hemorrhage / pathology
  • Homozygote
  • Humans
  • Hydrocephalus / etiology
  • Hydrocephalus / pathology
  • Infant, Newborn
  • Male
  • Protein C / analysis*
  • Protein C / genetics
  • Sinus Thrombosis, Intracranial / pathology
  • Thrombosis / etiology
  • Thrombosis / genetics
  • Thrombosis / pathology

Substances

  • Protein C