Samenvatting
Prenatal typing for the human platelet antigens-l (HPA) permits identification of a fetus at risk for neonatal alloimmune thrombocytopenia (NAITP) in cases of HPA-1 incompatibility in which the father is heterozygous for the HPA-la antigen. Diagnostic cordocentesis and phenotyping of the fetal platelets are used for this purpose. We applied allele-specific restriction enzyme analysis on polymerase chain reaction (PCR)-amplified DNA purified from amniocytes. This assay allows early second trimester typing for HPA-1 alleles. We were able to determine the genotype of three fetuses at risk. Iatrogenic fetal loss is lower with amniocentesis than with cordocentesis. Therefore, this technique is a welcome addition to the antenatal management of NAITP.
| Originele taal-2 | English |
|---|---|
| Pagina's (van-tot) | 15-19 |
| Aantal pagina's | 5 |
| Tijdschrift | Transfusion Medicine |
| Volume | 4 |
| Nummer van het tijdschrift | 1 |
| Status | Published - mrt.-1994 |
Vingerafdruk
Duik in de onderzoeksthema's van 'HUMAN PLATELET ANTIGEN-1 (ZW) TYPING OF FETUSES BY ANALYSIS OF POLYMERASE CHAIN REACTION-AMPLIFIED GENOMIC DNA FROM AMNIOCYTES'. Samen vormen ze een unieke vingerafdruk.Citeer dit
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