Prenatal Ultrasonographic Diagnosis of Klippel-Trenaunay-Weber Syndrome / 대한산부인과학회지
Korean Journal of Obstetrics and Gynecology
; : 1345-1352, 2006.
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.
Mots clés
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