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Prenatal Ultrasonographic Diagnosis of Klippel-Trenaunay-Weber Syndrome / 대한산부인과학회지
Article de Ko | WPRIM | ID: wpr-46633
Bibliothèque responsable: WPRO
ABSTRACT
Klippel-Trenaunay-Weber syndrome is a rare congenital disorders which is characterized by the presence of multiple hemangiomata, arteriovenous fistulas and unilateral limb hypertrophy. There has been some reports that Klippel-Trenaunay-Weber syndrome was diagnosed at birth or infant, but the prenatal diagnosis was very difficult in pregnant women who have not family history. Recently, the prenatal diagnosis of Klippel-Trenaunay-Weber syndrome has been occasionally reported according to improvement of prenatal ultrasound. We recently experienced two cases of Klippel-Trenaunay-Weber syndrome. So we report our cases with brief review of literature.
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Texte intégral: 1 Indice: WPRIM Sujet Principal: Diagnostic prénatal / Échographie / Fistule artérioveineuse / Syndrome de Klippel-Trénaunay / Parturition / Femmes enceintes / Diagnostic / Membres / Hypertrophie / Malformations et maladies congénitales, héréditaires et néonatales Type d'étude: Diagnostic_studies Limites du sujet: Female / Humans / Infant langue: Ko Texte intégral: Korean Journal of Obstetrics and Gynecology Année: 2006 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Diagnostic prénatal / Échographie / Fistule artérioveineuse / Syndrome de Klippel-Trénaunay / Parturition / Femmes enceintes / Diagnostic / Membres / Hypertrophie / Malformations et maladies congénitales, héréditaires et néonatales Type d'étude: Diagnostic_studies Limites du sujet: Female / Humans / Infant langue: Ko Texte intégral: Korean Journal of Obstetrics and Gynecology Année: 2006 Type: Article