Linked Life Data

21705736

Source:http://linkedlifedata.com/resource/pubmed/id/21705736

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2011-6-27
pubmed:abstractText
Records of 24 pregnancies with fetal polydactyly were reviewed for the type of polydactyly, family history, associated sonographic findings, genetic testing, and postnatal/postmortem examination findings. The importance of fetal polydactyly can be mainly elucidated by the family history and absent or associated anomalies on a specialized malformation scan. Fetal karyotyping diagnoses frequent chromosomal anomalies in about half of cases with additional malformations, and array comparative genomic hybridization may be a future means of detecting cryptic chromosomal aberrations. Syndromic disorders of monogenic origin demand a careful interdisciplinary clinical assessment for establishing a clinical diagnosis and prognosis for the outcome of the child.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1550-9613
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1021-9
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Fetal polydactyly: a study of 24 cases ascertained by prenatal sonography.
pubmed:affiliation
Division of Medical Genetics and Department of Biomedicine, University Children's Hospital, Burgfelderstrasse 101, Building J, 4005 Basel, Switzerland. isabel.filges@unibas.ch
pubmed:publicationType
Journal Article