Familial dysfunction of protein S

P. M. Mannucci, C. Valsecchi, A. Krachmalnicoff, E. M. Faioni, A. Tripodi

Research output: Contribution to journalArticlepeer-review

Abstract

We describe a previously unreported defect of protein S characterized by low levels of cofactor activity for activated protein C contrasting with low normal levels of total and free protein S antigen. The distribution of protein S between the free form and the form complexed with the complement component C4b-binding protein was normal on two-dimensional immunoelectrophoresis. The proband developed juvenile deep-vein thrombosis while taking oral contraceptives. Her defect was transmitted in an autosomal dominant fashion from her asymptomatic mother. Other relatives carrying the same laboratory abnormality (mother, maternal uncle, two sisters and one brother) were also asympatomatic. We postulate that the defect is due to a dysfunctional protein S present in plasma in normal amounts and with normal proportions of the free and complexed forms of the protein.

Original languageEnglish
Pages (from-to)763-766
Number of pages4
JournalThrombosis and Haemostasis
Volume62
Issue number2
Publication statusPublished - 1989

ASJC Scopus subject areas

  • Hematology

Fingerprint Dive into the research topics of 'Familial dysfunction of protein S'. Together they form a unique fingerprint.

Cite this