Thromb Haemost 1993; 70(02): 244-246
DOI: 10.1055/s-0038-1649477
Original Articles
Clinical Studies
Schattauer GmbH Stuttgart

Protein S Tokushima: An Abnormal Protein S Found in a Japanese Family with Thrombosis

Authors

  • T Shigekiyo

    1   The First Department of Internal Medicine, Mie University School of Medicine, Mie, Japan
  • Y Uno

    1   The First Department of Internal Medicine, Mie University School of Medicine, Mie, Japan
  • S Kawauchi

    1   The First Department of Internal Medicine, Mie University School of Medicine, Mie, Japan
  • S Saito

    1   The First Department of Internal Medicine, Mie University School of Medicine, Mie, Japan
  • H Hondo

    2   The Department of Neurological Surgery, School of Medicine, The University of Tokushima, Tokushima, Japan
  • J Nishioka

    3   The Department of Molecular Biology on Genetic Disease, Mie University School of Medicine, Mie, Japan
  • T Hayashi

    3   The Department of Molecular Biology on Genetic Disease, Mie University School of Medicine, Mie, Japan
  • K Suzuki

    3   The Department of Molecular Biology on Genetic Disease, Mie University School of Medicine, Mie, Japan
Further Information

Publication History

Received 27 July 1992

Accepted after revision 11 February 1993

Publication Date:
04 July 2018 (online)

Preview

Summary

An abnormal protein S (PS) was found in a Japanese family with a high incidence of thrombosis. The proband is a woman who was born in Tokushima Prefecture. She had superior sagittal sinus thrombosis, thrombophlebitis of the left leg, and thrombosis of the placenta. She had a normal plasma level of free PS antigen but decreased PS activity. Her mother and aunt also had thrombophlebitis of the leg, and together with four other family members also showed a normal level but decreased activity of PS. This suggests that hereditary dysfunction of PS is inherited in this family as an autosomal dominant trait. The proband’s PS appears to have a slightly higher molecular weight than normal PS both in the intact and modified form, suggesting that it has a molecular defect on the carboxyl-terminal side of the thrombin-sensitive site. This abnormal PS with apparently unique characteristics was named PS Tokushima.