Literature DB >> 21030308

Identification of anti-PP1P(k) in a blood donor and her family: a case report following her pregnancy and review.

Georgette R Benidt1, Elizabeth A Jaben, Jeffrey L Winters, James R Stubbs.   

Abstract

Anti-PP1P(k) is a rare, biphasic antibody with the ability to cause immediate hemolytic transfusion reactions and early spontaneous abortions. The antibody is formed by individuals with the p phenotype. A blood donor with anti-PP1P(k) and the p phenotype was identified through routine donor screening. A sister was found to also be p phenotype. At that time, the sister was 24weeks pregnant. Subsequently, the original blood donor became pregnant. Both individuals were followed throughout their pregnancies and delivered infants without complications from anti-PP1P(k) antibodies. The literature regarding anti-PP1P(k), the p phenotype, and recurrent pregnancy loss in this setting is reviewed.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21030308     DOI: 10.1016/j.transci.2010.10.009

Source DB:  PubMed          Journal:  Transfus Apher Sci        ISSN: 1473-0502            Impact factor:   1.764


  2 in total

1.  Deletion in the A4GALT Gene Associated with Rare "P null" Phenotype: The First Report from India.

Authors:  Shamee Shastry; Kapaettu Satyamoorthy; Kiran V Acharya; Vijay Ram Reddy; Ganesh Mohan; Chenna Deepika; Dinesh Reghunathan; Manjunath B Joshi
Journal:  Transfus Med Hemother       Date:  2019-08-21       Impact factor: 3.747

2.  Blood Group Discrepancies at a Regional Blood Center.

Authors:  Hayedeh Javadzadeh Shahshahani; Azam Hayati
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2020-01-01
  2 in total

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