Pregnancy complicated by hemoglobin CC and C-β-thalassemia disease

M. C. Maberry, R. A. Mason, F. G. Cunningham, J. A. Pritchard

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

The outcomes of 72 pregnancies in 20 women with either hemoglobin CC or C-β-thalassemia are described. Except for mild to moderate hemolytic anemia, maternal complications caused by the hemoglobinopathy were infrequent and perinatal outcomes were generally good. In eight women, blood volume expansion determined by51chromium-tagged erythrocytes was similar to that for normally pregnant women. Mean red-cell survival was determined 11 times in eight women, and the red-cell half-life of 22 days was significantly shorter than that of 35 days for normally pregnant women.

Original languageEnglish (US)
Pages (from-to)324-327
Number of pages4
JournalObstetrics and gynecology
Volume76
Issue number3
StatePublished - Sep 1990

ASJC Scopus subject areas

  • Obstetrics and Gynecology

Fingerprint Dive into the research topics of 'Pregnancy complicated by hemoglobin CC and C-β-thalassemia disease'. Together they form a unique fingerprint.

  • Cite this

    Maberry, M. C., Mason, R. A., Cunningham, F. G., & Pritchard, J. A. (1990). Pregnancy complicated by hemoglobin CC and C-β-thalassemia disease. Obstetrics and gynecology, 76(3), 324-327.