Abstract | BACKGROUND: Rare cases of hemolytic disease of the newborn occur in women with genetic variants of the D antigen. A partial D variant might be suspected when typing for the D antigen shows weaker-than-normal reactions (weak D). Historically, patients with a weak D phenotype have not been considered candidates for Rh immune globulin prophylaxis. CASE: A gravida 2, para 1 woman with A-positive blood type, delivered an infant who died from severe hemolytic disease of the newborn 6 days after birth. Anti-D, undetectable at the first prenatal visit, was identified (titer 1:64) at delivery. The mother's red cells were partial D(VI) phenotype. CONCLUSION: Although severe hemolytic disease in patients with partial D is rare, this neonatal death illustrates the need for a change in management of women with weak D.
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Authors | Michael Cannon, Richard Pierce, Evan Beth Taber, Jodi Schucker |
Journal | Obstetrics and gynecology
(Obstet Gynecol)
Vol. 102
Issue 5 Pt 2
Pg. 1143-5
(Nov 2003)
ISSN: 0029-7844 [Print] United States |
PMID | 14607035
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Isoantibodies
- Rh-Hr Blood-Group System
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Topics |
- Adult
- Erythroblastosis, Fetal
(etiology)
- Fatal Outcome
- Female
- Humans
- Hydrops Fetalis
(etiology)
- Isoantibodies
(immunology)
- Pregnancy
- Rh-Hr Blood-Group System
(immunology)
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