Severe Acquired Neonatal Purpura Fulminans

Abstract

Get full access to this article

View all access options for this article.

References

1. Branson HE , Katz J , Marble R , et al. Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant. Lancet. 1983;2:1165-1168.

2. Sills RH , Marlar RA , Montgomery RR , et al. Severe homozygous protein C deficiency.JPediatr. 1984;105:409-413.

3. Mahasandana C , Suvatte V , Chuansumrit A , et al. Homozygous protein S deficiency in an infant with purpura fulminans.JPediatr. 1990;117:750-753.

4. Hathaway WE , Bonnar J . Hemostatic Disorders of the Pregnant Woman and Newborn Infant. New York: Elsevier; 1987;57-75.

5. Manco-Johnson MJ , Abshire TC , Jacobson LJ , Marlar RA . Severe neonatal protein C deficiency: prevalence and thrombotic risk. J Pediatr. 1991; 119:793-798.

6. Laurell CB . Electroimmunoassay. ScandJ Clin Lab Invest. 1972;29 (Suppl 124):21-27.

7. Powars DR , Roger ZR , Patch MJ , et al. Purpura fulminans in meningococcemia: association with acquired deficiencies of protein C and S. NEnglJ Med. 1987;317:571-572.

8. Madden RM , Gill JC , Marlar R . Protein C and protein S levels in two patients with acquired purpura fulminans. BrJHaematol. 1990;75: 112-117.

9. Marlar RA , Montgomery RR , Broekmans AW , the Working Party. Diagnosis and treatment of homozygous protein C deficiency. Report of the working party on homozygous protein C deficiency of the subcommittee on protein C and protein S, International Committee on Thrombosis and Haemostatis. J Pediatr. 1989;114:528-534.

10.

10. Issacman SH , Heroman WM , Lightsey AL . Purpura fulminans following lateonset group B,B-hemolytic streptococcal sepsis. Am J Dis Child. 1984; 138:915-916.