Literature DB >> 87775

Plasma assay of fetal factors VIIIC and IX for prenatal diagnosis of haemophilia.

R S Mibashan, C H Rodeck, J K Thumpston, R J Edwards, J D Singer, J M White, S Campbell.   

Abstract

Fetal blood unmixed with maternal blood or amniotic fluid was obtained by direct-vision fetoscopy in 22 consecutive cases at 15--22 weeks' gestation; the investigation was done either for prenatal diagnosis or before therapeutic abortion. Fetal plasma factors VIIIC and IX averaged 50 I.U./dl (S.D. 12.8) and 12.5 I.U./dl (S.D. 2.4), respectively. Two male fetuses at risk of haemophilia had normal factor VIIIC levels by these criteria, and both pregnancies ended in the birth of a normal boy. Five others gave 3 normal and 2 haemophilic results, which were confirmed in two of the three terminated pregnancies.

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Year:  1979        PMID: 87775     DOI: 10.1016/s0140-6736(79)91946-9

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  12 in total

1.  Screening for mutations in the gene encoding factor IX.

Authors:  L R Nielsen; M Schwartz; E Scheibel
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Applications and limitations of direct DNA analysis in genetic prediction.

Authors:  M E Pembrey
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  The clinical relevance of factor VIII: C and factor VII R: Ag determination in newborns.

Authors:  R von Kries; H Jürgens; H von Voss; U Göbel
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

Review 4.  Recent advances in haematology.

Authors:  D Samson; I Chanarin; C D Reid
Journal:  Postgrad Med J       Date:  1981-03       Impact factor: 2.401

5.  Genetic counselling in haemophilia by discriminant analysis 1975-1980.

Authors:  E S Barrow; C H Miller; H M Reisner; J B Graham
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

6.  Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland.

Authors:  J M Connor; A F Pettigrew; I M Hann; C D Forbes; G D Lowe; N A Affara
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

7.  Value of fetoscopy in prenatal diagnosis.

Authors:  C H Rodeck
Journal:  J R Soc Med       Date:  1980-01       Impact factor: 5.344

8.  [New possibilities of heterozygote detection of hemophilia A].

Authors:  T L Boehm; J Svejcar; D Drahovsky
Journal:  Klin Wochenschr       Date:  1987-01-15

9.  Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism.

Authors:  E G Tuddenham; E Goldman; A McGraw; P B Kernoff
Journal:  J Clin Pathol       Date:  1987-09       Impact factor: 3.411

Review 10.  The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.

Authors:  A H Bröcker-Vriends; E Bakker; H H Kanhai; G J van Ommen; P H Reitsma; J J van de Kamp; E Briët
Journal:  Ann Hematol       Date:  1992-01       Impact factor: 3.673

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