Detection of subtelomeric aberrations as a cause of mental
retardation

a 2010

Detection of subtelomeric aberrations as a cause of mental retardation

ZRNOVÁ, Eva; Vladimíra VRANOVÁ; Renata GAILLYOVÁ a Petr KUGLÍK

Základní údaje

Originální název

Detection of subtelomeric aberrations as a cause of mental retardation

Název česky

Detekce subtelomerických aberací jako příčin mentální retardace

Autoři

ZRNOVÁ, Eva; Vladimíra VRANOVÁ; Renata GAILLYOVÁ a Petr KUGLÍK

Vydání

XIV. Pracovní setkání biochemiků a molekulárních biologů, 2010

Další údaje

Jazyk

angličtina

Typ výsledku

Konferenční abstrakt

Obor

Genetika a molekulární biologie

Stát vydavatele

Česká republika

Utajení

není předmětem státního či obchodního tajemství

Označené pro přenos do RIV

Organizační jednotka

Přírodovědecká fakulta

ISBN

978-80-210-5164-5

Klíčová slova česky

mentální retardace, subtelomerické aberace, MLPA

Klíčová slova anglicky

mental retardation, subtelomeric aberrations, MLPA

Změněno: 28. 4. 2011 13:35, RNDr. Vladimíra Vallová, Ph.D.

Anotace

V originále

Mental retardation (MR) is a various manifestation of dysfunction in the central nervous system. It is a major health care problem in developed countries affecting between 2-3% of population. It’s due to heterogeneous causes including environmental factors (15%), chromosomal abnormalities and monogenic disorders (30%). The cause of MR is unexplained in about 55% of cases. In the past few years it was emerged that a significant number of subtelomeric changes (about 5-8%) were detected in patients with idiopathic mental retardation as a cause of their disease using new sensitive methods of molecular cytogenetics as for example MLPA (Multiplex Ligation-dependent Probe Amplification). The detection of chromosomal rearrangements is usually done by routine analysis of G - banded metaphase chromosomes (karyotyping). It’s the basic cytogenetic method very important to detect balanced and imbalanced chromosomal changes. However, the G-band analysis has limited resolution and it can not detect aberration smaller than 5 Mb. The new methods of molecular cytogenetics have significantly increased this resolution. MLPA is one of the molecular methods used to uncover imbalanced changes (deletions and duplications). Due to a high cost of the whole genome screening methods, many studies analyze only a selected part of human genome – the physical ends of chromosomes (subtelomeres). This technique is based on PCR amplification of ligated probes hybridized to chromosome ends. Therefore MLPA was adapted for subtelomeric screening in patients with unexplained mental retardation in routine diagnostics. Over 160 patients with unexplained mental retardation were investigated using MLPA at Department of Medical Genetics, University Hospital Brno since 2007. We have detected 11 various subtelomeric aberrations (8 deletions and 5 duplications), suggesting a prevalence of 6,7% in our group of patients. This number of positive capture corresponds to international studies with the similar genetic focus.

Návaznosti

MSM0021622415, záměr

Název: Molekulární podstata buněčných a tkáňových regulací

Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Molekulární podstata buněčných a tkáňových regulací

Citovat

ZRNOVÁ, Eva; Vladimíra VRANOVÁ; Renata GAILLYOVÁ a Petr KUGLÍK. Detection of subtelomeric aberrations as a cause of mental retardation. In XIV. Pracovní setkání biochemiků a molekulárních biologů. 2010. ISBN 978-80-210-5164-5.

@proceedings{880717,
   author = {Zrnová, Eva and Vranová, Vladimíra and Gaillyová, Renata and Kuglík, Petr},
   booktitle = {XIV. Pracovní setkání biochemiků a molekulárních biologů},
   keywords = {mental retardation, subtelomeric aberrations, MLPA},
   language = {eng},
   isbn = {978-80-210-5164-5},
   title = {Detection of subtelomeric aberrations as a cause of mental retardation},
   year = {2010}
}

TY  - CONF
ID  - 880717
AU  - Zrnová, Eva - Vranová, Vladimíra - Gaillyová, Renata - Kuglík, Petr
PY  - 2010
TI  - Detection of subtelomeric aberrations as a cause of mental retardation
SN  - 9788021051645
KW  - mental retardation, subtelomeric aberrations, MLPA
N2  - Mental retardation (MR) is a various manifestation of dysfunction in the central nervous system. It is a major health care problem in developed countries affecting between 2-3% of population. It’s due to heterogeneous causes including environmental factors (15%), chromosomal abnormalities and monogenic disorders (30%). The cause of MR is unexplained in about 55% of cases. In the past few years it was emerged that a significant number of subtelomeric changes (about 5-8%) were detected in patients with idiopathic mental retardation as a cause of their disease using new sensitive methods of molecular cytogenetics as for example MLPA (Multiplex Ligation-dependent Probe Amplification). The detection of chromosomal rearrangements is usually done by routine analysis of G - banded metaphase chromosomes (karyotyping). It’s the basic cytogenetic method very important to detect balanced and imbalanced chromosomal changes. However, the G-band analysis has limited resolution and it can not detect aberration smaller than 5 Mb. The new methods of molecular cytogenetics have significantly increased this resolution. MLPA is one of the molecular methods used to uncover imbalanced changes (deletions and duplications). Due to a high cost of the whole genome screening methods, many studies analyze only a selected part of human genome – the physical ends of chromosomes (subtelomeres). This technique is based on PCR amplification of ligated probes hybridized to chromosome ends. Therefore MLPA was adapted for subtelomeric screening in patients with unexplained mental retardation in routine diagnostics. Over 160 patients with unexplained mental retardation were investigated using MLPA at Department of Medical Genetics, University Hospital Brno since 2007. We have detected 11 various subtelomeric aberrations (8 deletions and 5 duplications), suggesting a prevalence of 6,7% in our group of patients. This number of positive capture corresponds to international studies with the similar genetic focus.
ER  -

ZRNOVÁ, Eva; Vladimíra VRANOVÁ; Renata GAILLYOVÁ a Petr KUGLÍK. Detection of subtelomeric aberrations as a cause of mental retardation. In \textit{XIV. Pracovní setkání biochemiků a molekulárních biologů}. 2010. ISBN~978-80-210-5164-5.

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