Literature DB >> 3219292

Thrombovascular disease and familial plasminogen deficiency: a report of three kindreds.

G Dolan1, M Greaves, P Cooper, F E Preston.   

Abstract

We report three kindreds in whom plasminogen deficiency was associated with thrombosis and in whom the ratio of functional and immunological values of plasminogen was consistent with type I deficiency. An additional subject with plasminogen deficiency is also described. The three propositi presented with venous thrombotic disease. The fourth subject presented with a thrombotic stroke. Investigation of family members in three of these four cases revealed other subjects who were found to have low levels of plasminogen and who were asymptomatic. The pattern of inheritance appears to be autosomal dominant. In one woman, plasminogen levels were shown to rise to within the normal range during pregnancy and returned to low levels after delivery. A total of eight pregnancies were reviewed in our series and no thrombotic events occurred.

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Year:  1988        PMID: 3219292     DOI: 10.1111/j.1365-2141.1988.tb02510.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  3 in total

Review 1.  Guidelines on the investigation and management of thrombophilia. The British Committee for Standards in Haematology.

Authors: 
Journal:  J Clin Pathol       Date:  1990-09       Impact factor: 3.411

2.  Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis.

Authors:  A Ichinose; E S Espling; J Takamatsu; H Saito; K Shinmyozu; I Maruyama; T E Petersen; E W Davie
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

Review 3.  Genetics and pulmonary medicine. 4. Pulmonary embolism.

Authors:  M Laffan
Journal:  Thorax       Date:  1998-08       Impact factor: 9.139

  3 in total

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