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Tetrasomy 9p Mosaicism Associated with a Normal Phenotype in Two Cases

  • Tetrasomy 9p is a rare chromosomal syndrome and about 30% of known cases exhibit mosaicism. Approximately 50 of the reported cases with tetrasomy 9p mosaicism show a characteristic facial appearance, growth failure, and developmental delay. However, 3 patients with mosaicism for isochromosome 9p and a normal phenotype have also been reported. We report 2 additional cases of clinically normal young females with tetrasomy 9p mosaicism, one of whom also exhibited X chromosome aneuploidy mosaicism leading to an overall of 6 different cell lines. STR analysis performed on this complex mosaic case indicated that the extra isochromosome was of maternal origin while the X chromosome aneuploidy was of paternal origin, indicating a postzygotic event.

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Author: I. Papoulidis, M. Kontodiou, M. Tzimina, I. Saitis, A.B. Hamid, E. Klein, N. Kosyakova, U. Kordaß, J. Kunz, E. Siomou, P. Nicolaides, S. Orru, L. Thomaidis, T. Liehr, M.B. Petersen, E. Manolakos
URN:urn:nbn:de:gbv:9-opus-31471
DOI:https://doi.org/10.1159/000337520
ISSN:1424-8581
ISSN:1424-859X
Pubmed Id:https://pubmed.ncbi.nlm.nih.gov/22487875
Parent Title (English):Cytogenetic and Genome Research
Publisher:S. Karger AG
Place of publication:Basel, Switzerland
Document Type:Article
Language:English
Date of first Publication:2012/04/05
Release Date:2020/09/29
Tag:Mosaicism; Normal phenotype; Tetrasomy 9p
GND Keyword:-
Volume:136
Issue:4
First Page:237
Last Page:241
Faculties:Universitätsmedizin / Institut für Humangenetik
Licence (German):License LogoUrheberrechtlich geschützt