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Prenatal Ultrasonographic Diagnosis of Klippel-Trenaunay-Weber Syndrome / 대한산부인과학회지
Korean Journal of Obstetrics and Gynecology ; : 1345-1352, 2006.
Article in Korean | WPRIM | ID: wpr-46633
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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Full text: Available Index: WPRIM (Western Pacific) Main subject: Prenatal Diagnosis / Ultrasonography / Arteriovenous Fistula / Klippel-Trenaunay-Weber Syndrome / Parturition / Pregnant Women / Diagnosis / Extremities / Hypertrophy / Congenital, Hereditary, and Neonatal Diseases and Abnormalities Type of study: Diagnostic study Limits: Female / Humans / Infant Language: Korean Journal: Korean Journal of Obstetrics and Gynecology Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Prenatal Diagnosis / Ultrasonography / Arteriovenous Fistula / Klippel-Trenaunay-Weber Syndrome / Parturition / Pregnant Women / Diagnosis / Extremities / Hypertrophy / Congenital, Hereditary, and Neonatal Diseases and Abnormalities Type of study: Diagnostic study Limits: Female / Humans / Infant Language: Korean Journal: Korean Journal of Obstetrics and Gynecology Year: 2006 Type: Article