| Congenital disorders of glycosylation type Ia as a cause of mirror syndrome. | |
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MedLine Citation:
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PMID: 18034167 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Mirror syndrome (that is fetal hydrops with subsequent edema in the pregnant woman) is a rare condition. Early diagnosis is warranted, as maternal and fetal morbidity and mortality is increased if not diagnosed and treated properly. In most cases, the underlying cause remains unclear. We report a woman who has had two pregnancies complicated by mirror syndrome. Congenital disorder of glycosylation type Ia (CDG-Ia) was identified as the underlying fetal disease in both cases. |
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Authors:
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D Wurm; G Löffler; A Lindinger; L Gortner |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Journal of perinatology : official journal of the California Perinatal Association Volume: 27 ISSN: 0743-8346 ISO Abbreviation: J Perinatol Publication Date: 2007 Dec |
Date Detail:
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Created Date: 2007-11-23 Completed Date: 2008-02-08 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8501884 Medline TA: J Perinatol Country: United States |
Other Details:
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Languages: eng Pagination: 802-4 Citation Subset: IM |
Affiliation:
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Department of Pediatrics and Neonatology, University Children's Hospital, Homburg/Saar, Germany. donaldwurm@freenet.de |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Carbohydrate Metabolism, Inborn Errors
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complications*,
diagnosis*,
genetics Female Glycosylation Humans Hydrops Fetalis / etiology* Infant, Newborn Male Pregnancy |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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