Literature DB >> 6130994

Hypogammaglobulinaemia during pregnancy in identical twin sisters.

Z O Amarin, K A Grant.   

Abstract

The clinical histories and reaction to pregnancy is described in identical twin sisters with acquired hypogammaglobulinemia. Additional evidence for the genetic basis of this disorder is advanced. A possible association with myasthenia gravis is noted and the occurrence of fetal growth retardation is described. Replacement therapy should be given when the diagnosis is made, and high doses might be useful during pregnancy especially if fetal growth retardation seems to be present.

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Year:  1982        PMID: 6130994     DOI: 10.1016/0020-7292(82)90008-x

Source DB:  PubMed          Journal:  Int J Gynaecol Obstet        ISSN: 0020-7292            Impact factor:   3.561


  3 in total

Review 1.  Genetics of IgA deficiency and common variable immunodeficiency.

Authors:  H W Schroeder
Journal:  Clin Rev Allergy Immunol       Date:  2000-10       Impact factor: 8.667

2.  IgG replacement therapy for primary hypogammaglobulinaemia during pregnancy: report of 9 pregnancies in 4 patients.

Authors:  P E Williams; C L Leen; A D Heppleston; P L Yap
Journal:  Blut       Date:  1990-03

3.  Intravenous immunoglobulin replacement therapy for common variable immunodeficiency during pregnancy.

Authors:  H Osada; Y Morikawa; T Nishiwaki; S Sekiya
Journal:  Arch Gynecol Obstet       Date:  1996       Impact factor: 2.344

  3 in total

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