|
|
| Research article summary (published 29 Apr 1991): |
[Pätau syndrome without trisomy karyotype? Danger of restricted thinking in syndrome diagnosis]
(PATAU-SYNDROM ohne Trisomie-Karyotyp? Die Gefahr des "Schubladendenkens" in der Syndromdiagnostik.)
Full Abstract
By means of a case-report the problems of an uncritical usage of the terminus "syndrom" are pointed out. The report concerns with a newborn child clinically showing nearly all morphological characteristics of the "Pätau-Syndrom" without having a chromosomal aberration.
Author information
Author/s: Rode, G (G); Duda, V (V);
Affiliation: Universitäts-Frauenklinik Marburg.
Journal and publication information
Publication Type: Case Reports; English Abstract; Journal Article
Journal: Zeitschrift für Geburtshilfe und Perinatologie (Z Geburtshilfe Perinatol), published in GERMANY. (Language: ger)
Reference: -1991 May-Jun; vol 195 (issue 3) : pp 143-5
Dates: Created 1991/11/12; Completed 1991/11/12; Revised 2006/11/15;
PMID: 1926974, status: MEDLINE (last retrieved date: 2/18/2009)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
External Links for this article
(including full text providers, if available):
Click Electronic Full-text Provider Links to see options for finding the electronic full text links to this article. Note there may be a subscription or fee required for access to the full text. See our FAQ for information on finding FREE full text articles.
This article may also be located in paper journal collections available in many libraries. Use the Journal and Publication Information above to find the full article.
MeSH headings (categories)
This article was linked to the MeSH Headings (categories) shown below.
Note: Bold headings indicate primary MeSH headings or qualifiers.
Related articles
These are the most related articles currently in our database:
- Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
30 Mar 2005 - Prenatal diagnosis of trisomy 6 mosaicism.
29 Apr 2005 - Postzygotic isochromosome formation as a cause for false-negative results from chorionic villus chromosome examinations.
27 Feb 2006 - Molecular cytogenetic investigation of a balanced complex chromosomal rearrangement carrier ascertained through a neonate with partial trisomies of 13 and 22.
29 Jun 2007 - Prenatal diagnosis of monosomy 4p14-->pter and trisomy 11q25-->qter: clinical presentations and outcomes.
29 Nov 2005 - Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe.
30 Oct 2004 - Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?
30 Jul 2005 - Complete trisomy 1q with mosaic Y;1 translocation: a recurrent aneuploidy presenting diagnostic dilemmas.
29 Sep 2005 - Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.
30 Dec 2006 - Trisomy 18: a case study.
30 Dec 2007
Related Article Map
Legend:
- FREE Full text Article.
- Abstract only.
- Title only. More help.
See a larger map of 100+ related articles.