Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
9
|
| pubmed:dateCreated |
1989-10-31
|
| pubmed:abstractText |
We describe a case in which a trisomic 22 placenta could be the cause of severe growth retardation in a chromosomally normal female fetus. At amniocentesis a mosaic 46,XX/47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cordocentesis revealed a normal chromosome constitution. Postnatal studies showed the consistent presence of trisomic 22 cells in the placenta, while only normal metaphases were found in amnion, blood, and fibroblast cultures.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Sep
|
| pubmed:issn |
0197-3851
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
9
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
673-6
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:2798352-Chorionic Villi,
pubmed-meshheading:2798352-Chromosomes, Human, Pair 22,
pubmed-meshheading:2798352-Female,
pubmed-meshheading:2798352-Fetal Growth Retardation,
pubmed-meshheading:2798352-Humans,
pubmed-meshheading:2798352-Karyotyping,
pubmed-meshheading:2798352-Middle Aged,
pubmed-meshheading:2798352-Mosaicism,
pubmed-meshheading:2798352-Placenta Diseases,
pubmed-meshheading:2798352-Pregnancy,
pubmed-meshheading:2798352-Trisomy
|
| pubmed:year |
1989
|
| pubmed:articleTitle |
Trisomic 22 placenta in a case of severe intrauterine growth retardation.
|
| pubmed:affiliation |
Laboratorio di Citogenetica, Instituti Clinici di Perfezionamento, Milano, Italy.
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|