Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.

The single-exon approach for fetal RHD screening early in pregnancy is an appropriate choice in the population of Western Sweden, with a very low frequency of inconclusive results caused by the presence of maternal RHD gene variants. Due to the high sensitivity, specificity, and accuracy of the test, serological typing of neonates born to RhD negative women has no longer been performed at our laboratory since June 2023.

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Publication Details

Journal
PubMed
Published
2024-09-01
DOI
https://doi.org/10.2450/bloodtransfus.741
Citations
1
Primary Topic
Prenatal Screening and Diagnostics
Type
article
Field-Weighted Citation Impact
1.11

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article

Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.

Åsa Hellberg, Pauline Isakson, Cecilia Pardi
1 citations
PubMed
Prenatal Screening and Diagnostics
1.11
article

Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.

Åsa Hellberg, Pauline Isakson, Cecilia Pardi
article en
1 citations

Abstract

The single-exon approach for fetal RHD screening early in pregnancy is an appropriate choice in the population of Western Sweden, with a very low frequency of inconclusive results caused by the presence of maternal RHD gene variants. Due to the high sensitivity, specificity, and accuracy of the test, serological typing of neonates born to RhD negative women has no longer been performed at our laboratory since June 2023.

PubMedVol. 22(5)
Sahlgrenska University Hospital (SE)
Sahlgrenska Universitetssjukhuset
Good health and well-being
Openalex Percentile: Top 21%
Prenatal Screening and Diagnostics
1.11
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