Literature DB >> 3988955

A bleeding disorder due to deficiency of alpha 2-antiplasmin.

P Kettle, E E Mayne.   

Abstract

The investigation of a 33 year old man with a lifelong bleeding tendency is described. Defective fibrinolysis was suspected in 1968, when clinical bleeding was corrected by administration of aminocaproic acid. The paper establishes the diagnosis as alpha 2-antiplasmin deficiency and describes its management with oral tranexamic acid.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3988955      PMCID: PMC499170          DOI: 10.1136/jcp.38.4.428

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  5 in total

1.  The mechanism of clot dissolution by plasmin.

Authors:  N ALKJAERSIG; A P FLETCHER; S SHERRY
Journal:  J Clin Invest       Date:  1959-07       Impact factor: 14.808

2.  Electroimmuno assay.

Authors:  C B Laurell
Journal:  Scand J Clin Lab Invest Suppl       Date:  1972

3.  Quantitative estimation of split products of fibrinogen in human serum, relation to diagnosis and treatment.

Authors:  C Merskey; G J Kleiner; A J Johnson
Journal:  Blood       Date:  1966-07       Impact factor: 22.113

4.  A familial hemorrhagic diathesis in a Dutch family: an inherited deficiency of alpha 2-antiplasmin.

Authors:  C Kluft; E Vellenga; E J Brommer; G Wijngaards
Journal:  Blood       Date:  1982-06       Impact factor: 22.113

5.  Alpha2-plasmin-inhibitor deficiency (Miyasato disease).

Authors:  K Koie; T Kamiya; K Ogata; J Takamatsu
Journal:  Lancet       Date:  1978 Dec 23-30       Impact factor: 79.321

  5 in total
  1 in total

Review 1.  Clinical disorders of fibrinolysis: a critical review.

Authors:  R B Francis
Journal:  Blut       Date:  1989-07
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.