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Gewählte Publikation:

Petek, E; Pertl, B; Tschernigg, M; Bauer, M; Mayr, J; Wagner, K; Kroisel, PM.
Characterisation of a 19-year-old long-term survivor with Edwards syndrome.
Genet Couns. 2003; 14(2):239-244 (- Case Report)
Web of Science PubMed

 

Führende Autor*innen der Med Uni Graz
Kroisel Peter
Petek Erwin
Co-Autor*innen der Med Uni Graz
Holzapfel-Bauer Margit
Mayr Johannes
Pertl Barbara
Tschernigg Michaela
Wagner Klaus
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Abstract:
Trisomy 18 is the second most frequent autosomal aneuploidy affecting about 1 in 8,000 new-borns. Similar to trisomy 13 more than 90% of the patients die within the first year. Main causes of death are failure of vital organ function, in most cases of brain, heart, kidney, and gut, sometimes combined with severe infections. The degree to which essential organs are affected at birth and the clinical course differ considerably. Unknown genetic factors and various environmental effects are most likely involved. A less severe course of Edwards syndrome can be caused by a partial trisomy due to a deletion of the extra chromosome 18 or somatic mosaicism with a trisomic and a normal cell-line in the patient. In this report conventional chromosome analysis, FISH, and QF-PCR have been performed on a 19-year-old female patient with trisomy 18 to investigate a large number of cells including non-mitotic cells from various different tissues. This study supports evidence for an apparently pure form of trisomy 18 in this "long-living" patient with Edwards syndrome.
Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Aneuploidy -
Chromosome Mapping -
Chromosomes, Human, Pair 13 - genetics
Chromosomes, Human, Pair 18 - genetics
Female - genetics
Humans - genetics
Polymerase Chain Reaction - genetics
Survival Rate - genetics
Syndrome - genetics
Trisomy - genetics

Find related publications in this database (Keywords)
Edwards syndrome
fluorescence in situ hybridisation
long term survivor
mosaic
QF-PCR
trisomy 18
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