Korean J Obstet Gynecol.  2006 Jun;49(6):1345-1352.

Prenatal Ultrasonographic Diagnosis of Klippel-Trenaunay-Weber Syndrome

Affiliations
  • 1Department of Obstetrics and Gynecology, Busan Paik Hospital, College of Medicine, Inje University, Busan, Korea. fluro@hanmail.net
  • 2Department of Pathology, Busan Paik Hospital, College of Medicine, Inje University, Busan, Korea.

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.

Keyword

Klippel-trenaunay-weber syndrome; Prenatal diagnosis; Ultrasonography

MeSH Terms

Arteriovenous Fistula
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Diagnosis*
Extremities
Female
Humans
Hypertrophy
Infant
Klippel-Trenaunay-Weber Syndrome*
Parturition
Pregnant Women
Prenatal Diagnosis
Ultrasonography
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