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.
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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