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@proceedings{950057,
author = {Hanáková, Marta and Zrnová, Eva and Vranová, Vladimíra and Prášilová, Šárka and Kalina, Zdeněk and Filková, Hana and Tomášiková, Lenka and Vilémová, Marcela and Peťovská, Pavlína and Makaturová, Eva and Unucková, Markéta and Kuglík, Petr and Valášková, Iveta and Frengen, Eirik and Gaillyová, Renata},
booktitle = {8th European Cytogenetics Conference},
keywords = {complex chromosomal rearrangements, molecular cytogenetic methods},
title = {Rare Constitutional Chromosomal Rearrangements Found In Three Probands},
year = {2011}
}
TY - CONF
ID - 950057
AU - Hanáková, Marta - Zrnová, Eva - Vranová, Vladimíra - Prášilová, Šárka - Kalina, Zdeněk - Filková, Hana - Tomášiková, Lenka - Vilémová, Marcela - Peťovská, Pavlína - Makaturová, Eva - Unucková, Markéta - Kuglík, Petr - Valášková, Iveta - Frengen, Eirik - Gaillyová, Renata
PY - 2011
TI - Rare Constitutional Chromosomal Rearrangements Found In Three Probands
KW - complex chromosomal rearrangements, molecular cytogenetic methods
N2 - Complex chromosomal rearrangements (CCRs) are characterized as rare reciprocal exchanges between three or more chromosomes with at least three breakpoints. Apparently balanced CCRs can be associated with mental retardation and congenital abnormalities. In some cases these abnormalities can be caused by submicroscopic deletions or duplications which is possible to detect by high resolution molecular cytogenetic methods. In our work we present clinical, cytogenetic and molecular cytogenetic findings of three patients with rare constitutional chromosomal rearrangements. Two of them can be included in group CCRs, the third patient has an unusual chromosomal exchange which involves three chromosomes, but only two breakpoints. This rearrangement was not reciprocal and simulated a simple reciprocal translocation t(7;18) on G-banded chromosomes. For precise identification of these chromosomal rearrangements we used G-banding, SKY, FISH, CGH, HR-CGH and oligonucleotide based array-CGH techniques. Proband 1 was a 7-year-old girl with stigmatisation, mental retardation and autism. We detected apparently balanced karyotype 46,XX,der(2)t(2;5),der(5)t(2;5;10),der(10)t(2;10)de novo. Proband 2 was a newborn stigmatised boy, we revealed familiar apparently balanced karyotype with double two way translocation 46,XY,t(1;14)(p34;q24),t(4;6)(q25;p23)pat. Proband 3 was a newborn boy without significant anomalies, growth retardation was developed later. Karyotype of this patient was 46,XY,der(7)t(6;7)(q25.3;q21.2),der(18)t(7;18)(q21.2;q22.3)del(18)(q23?-qter)de novo. We conclude that it is necessary to use all available classical and molecular cytogenetic methods for clarification of complex and unusual chromosomal exchages and verification of suspect imbalances.
ER -
HANÁKOVÁ, Marta, Eva ZRNOVÁ, Vladimíra VRANOVÁ, Šárka PRÁŠILOVÁ, Zdeněk KALINA, Hana FILKOVÁ, Lenka TOMÁŠIKOVÁ, Marcela VILÉMOVÁ, Pavlína PEŤOVSKÁ, Eva MAKATUROVÁ, Markéta UNUCKOVÁ, Petr KUGLÍK, Iveta VALÁŠKOVÁ, Eirik FRENGEN a Renata GAILLYOVÁ. Rare Constitutional Chromosomal Rearrangements Found In Three Probands. Online. In \textit{8th European Cytogenetics Conference}. 2011. ISSN~0967-3849. [citováno 2024-04-23]
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