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Am J Med Genet A ; 120A(4): 528-32, 2003 Aug 01.
Article in English | MEDLINE | ID: mdl-12884433

ABSTRACT

Congenital anomalies of the umbilical and portal venous system are rare vascular malformations which are often associated with anomalies of the heart and gastrointestinal tract. Association with chromosomal disorders has been sporadically reported. We now report on two patients with trisomy 21 and congenital anomalies of the umbilico-portal system. A male fetus showed absence of the intrahepatic portal vein (PV) and ductus venosus with a direct communication between portal sinus and inferior vena cava exhibiting an umbilicosystemic total shunt during the fetal life and a portosystemic total shunt after birth. A female infant showed absence of the intrahepatic PV and a total portocaval shunt. Both patients also had heart defects. As previously documented in other reports, our cases demonstrated that this association may be causally-related to the chromosomal aberration. In addition, the umbilico-portal venous system abnormalities seems to be the most frequent congenital vascular malformation in Down syndrome. A presumptive pathogenetic mechanism could be a trisomy 21-related altered angiogenesis of the vitelloumbilical plexus.


Subject(s)
Abnormalities, Multiple/diagnostic imaging , Down Syndrome/complications , Portal Vein/abnormalities , Umbilical Veins/abnormalities , Abnormalities, Multiple/genetics , Adult , Child , Down Syndrome/genetics , Female , Humans , Infant , Male , Portal System/abnormalities , Portal System/diagnostic imaging , Portal Vein/diagnostic imaging , Pregnancy , Ultrasonography, Prenatal , Umbilical Veins/diagnostic imaging , Vena Cava, Inferior/abnormalities , Vena Cava, Inferior/diagnostic imaging
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