| Klippel-Trénaunay-Weber syndrome associated with fetal growth restriction. | |
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MedLine Citation:
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PMID: 8981152 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Klippel-Trénaunay-Weber syndrome is a rare congenital deep-vein malformation. Pregnancy in patients with this syndrome is rare and only a few cases have been reported. Known obstetrical risks in pregnant patients with this syndrome include bleeding from angiomata in the genitalia, and coagulation disturbances. We present a 31 year old woman with this syndrome who, on two occasions, delivered small-for-gestational-age neonates. This may have been due to placental insufficiency caused by angiomatosis related to the syndrome. |
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Authors:
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G Fait; Y Daniel; M J Kupferminc; I Gull; M R Peyser; J B Lessing |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Human reproduction (Oxford, England) Volume: 11 ISSN: 0268-1161 ISO Abbreviation: Hum. Reprod. Publication Date: 1996 Nov |
Date Detail:
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Created Date: 1997-03-20 Completed Date: 1997-03-20 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 8701199 Medline TA: Hum Reprod Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 2544-5 Citation Subset: IM |
Affiliation:
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Department of Obstetrics and Gynecology A, Serlin Maternity Hospital, Tel Aviv Sourasky Medical Center, Israel. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adult Female Fetal Growth Retardation / etiology* Humans Klippel-Trenaunay-Weber Syndrome / complications*, pathology Placenta / blood supply, pathology Pregnancy Pregnancy Complications* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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