Literature DB >> 3494989

Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood sampling.

G Corney, D B Whitehouse, D A Hopkinson, C H Rodeck, K Nicolaides, M Norman, A P Mowat.   

Abstract

Fetal blood sampling for the diagnosis of alpha-1-antitrypsin deficiency using protein isoelectric focusing was carried out in the period 1980-1985. The results of 25 cases from 18 mothers are reported. All had a previous history of a PiZ child affected by liver disease. The method was found to be technically satisfactory and the fetal results were subsequently confirmed in all 18 cases where follow-up was possible. The fetus was found to be PiZ in nine cases and all these pregnancies were terminated. Of the remaining pregnancies three cases aborted or were delivered prematurely and 13 proceeded to term without complications.

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Year:  1987        PMID: 3494989     DOI: 10.1002/pd.1970070206

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  Genetics and lung disease.

Authors:  D C Hutchison
Journal:  BMJ       Date:  1991-07-20

Review 2.  Liver disease in infancy: a 20 year perspective.

Authors:  G Mieli-Vergani; E R Howard; A P Mowat
Journal:  Gut       Date:  1991-09       Impact factor: 23.059

Review 3.  Alpha 1-antitrypsin deficiency and liver disease: clinical presentation, diagnosis and treatment.

Authors:  M Hussain; G Mieli-Vergani; A P Mowat
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

  3 in total

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