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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1984-10-25
|
| pubmed:abstractText |
A 20-day-old female neonate was admitted with symptoms caused by a large ventricular septal defect which was subsequently confirmed angiographically. Other clinical findings were pre- and postnatal growth retardation, microcephaly, dysmorphism of ears, fingers and feet. Cytogenetic analysis revealed a ring chromosome 15. Despite a palliative banding operation of the pulmonary artery, the infant succumbed to complications of her congenital heart disease in the 4th month of life.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
0340-6199
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
142
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
229-31
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:6468449-Abnormalities, Multiple,
pubmed-meshheading:6468449-Chromosome Aberrations,
pubmed-meshheading:6468449-Chromosome Disorders,
pubmed-meshheading:6468449-Chromosomes, Human, 13-15,
pubmed-meshheading:6468449-Female,
pubmed-meshheading:6468449-Growth Disorders,
pubmed-meshheading:6468449-Heart Septal Defects, Ventricular,
pubmed-meshheading:6468449-Humans,
pubmed-meshheading:6468449-Infant,
pubmed-meshheading:6468449-Intestines
|
| pubmed:year |
1984
|
| pubmed:articleTitle |
Dysplastic features, growth retardation, malrotation of the gut, and fatal ventricular septal defect in a 4-month-old girl with ring chromosome 15.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|