| Literature DB >> 11451561 |
T Fischer1, G Wallukat, M P Schneider, D Schlembach, W Munz, V Homuth.
Abstract
We present a 24-year-old woman with a twin pregnancy who was with a typical HELLP syndrome at the 18th week of pregnancy. One fetus was dead, while the other was severely growth retarded. Our patient had agonistic autoantibodies directed at the angiotensin AT(1)-receptor. Termination of the pregnancy proved necessary. This report is the first to our knowledge associating HELLP syndrome with angiotensin AT(1)-receptor antibodies. Since the antibodies may have a pathogenic significance, their removal could permit the prolongation of pregnancy in preeclamptic and HELLP syndrome patients.Entities:
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Year: 2001 PMID: 11451561 DOI: 10.1016/s0301-2115(00)00534-0
Source DB: PubMed Journal: Eur J Obstet Gynecol Reprod Biol ISSN: 0301-2115 Impact factor: 2.435