Linked Life Data

8260080

Source:http://linkedlifedata.com/resource/pubmed/id/8260080

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1994-1-25
pubmed:abstractText
A case is presented in which ultrasonographic examination led to the prenatal detection of a ring 13 chromosome in a fetus. At 18 weeks' gestation, the fetus presented with holoprosencephaly, an abnormal configuration of the lower extremities, and an atrial septal defect. Although the amount of amniotic fluid was normal, limb movements were never observed throughout pregnancy. The lower extremities were always flexed at the knee and talipes equinovarus was present. Hydrocephaly became apparent during the 2nd trimester. The ultrasonographic findings were confirmed by postpartum autopsy and X-ray examination. The ring chromosome was identified through amniocentesis and later verified in postpartum tissue.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
1015-3837
pubmed:author
pubmed:issnType
Print
pubmed:volume
8
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
261-7
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed:articleTitle
Ultrasonographic prenatal diagnosis of the 13q-syndrome.
pubmed:affiliation
Department of Obstetrics and Gynecology, University of Illinois at Chicago 60612.
pubmed:publicationType
Journal Article, Case Reports