Literature DB >> 871417

A CRM-Positive variant of factor-VII deficiency and the detection of heterozygotes with the assay of factor-like antigen.

M G Mazzucconi, F Mandelli, G Mariani, E Briët, J J Veltkamp.   

Abstract

Nine patients with severe factor-VII deficiency, belonging to seven pedigrees were studied for the presence of factor-VII-CRM with an inhibitor neutralization assay. The antibody, raised in rabbits, did not precipitate the antigen and could only be used in a fluid phase assay to measure the capacity of plasma to neutralize inhibitory activity directed against factor-VII activity. In one of these nine patients normal amounts of factor-VII-CRM could be demonstrated. The CRM + patient did not show a clinical picture at variance with that of the CRM-patients. The investigation into this CRM+ pedigree revealed heterozygosity in nine out of 12 persons when using the ratio between biological factor-VII activity and factor-VII-CRM as the criterion.

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Year:  1977        PMID: 871417     DOI: 10.1111/j.1365-2141.1977.tb05762.x

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


  3 in total

1.  Studies on a family with the factor VII defect.

Authors:  W D Zwierzina; F Kunz; J Glatzl
Journal:  Blut       Date:  1983-01

2.  Congenital factor VII deficiency. A report of four new cases.

Authors:  R Zimmermann; G Ehlers; W Ehlers; H von Voss; U Göbel; U Wahn
Journal:  Blut       Date:  1979-02-19

3.  Further studies on factor VII Padua defect: the report of the fourth homozygous patient from the same valley.

Authors:  A Girolami; A Gaio; L Doglioni; M Procidano; P Saltarin
Journal:  Blut       Date:  1982-06
  3 in total

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