| Prenatal diagnosis of the Klippel-Trenaunay-Weber syndrome. | |
| | |
MedLine Citation:
|
PMID: 7899273 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
The Klippel-Trenaunay-Weber syndrome is a complex developmental disorder of the vascular and skeletal systems. While many features of the syndrome are congenital, it has not been diagnosed often before birth. This paper describes a case of Klippel-Trenaunay-Weber syndrome diagnosed at 19 weeks' gestation on the basis of sonographic findings and family history. The clinical variability of the syndrome is emphasized and the importance of family history in differential diagnosis is stressed. |
| | |
Authors:
|
R J Jorgenson; B Darby; R Patterson; K J Trimmer |
Related Documents
:
|
19889273 - Klippel-trenaunay syndrome. 4073253 - Aural abnormalities in klippel-feil syndrome. 6698063 - Familial digeorge syndrome with tetralogy of fallot and prolonged survival. |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Prenatal diagnosis Volume: 14 ISSN: 0197-3851 ISO Abbreviation: Prenat. Diagn. Publication Date: 1994 Oct |
Date Detail:
|
Created Date: 1995-04-27 Completed Date: 1995-04-27 Revised Date: 2004-11-17 |
Medline Journal Info:
|
Nlm Unique ID: 8106540 Medline TA: Prenat Diagn Country: ENGLAND |
Other Details:
|
Languages: eng Pagination: 989-92 Citation Subset: IM |
Affiliation:
|
Central Texas Genetics Center, Austin 78756. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adult Family Health Female Fetal Diseases / diagnosis*, ultrasonography Humans Klippel-Trenaunay-Weber Syndrome / diagnosis*, ultrasonography Male Pregnancy Pregnancy Trimester, Second Prenatal Diagnosis* Ultrasonography, Prenatal |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Hyperechoic fetal bowel: the perinatal consequences.
Next Document: Intrauterine intervention in a case of recurrent meconium peritonitis.