Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10107123" target="_blank" >RIV/00216208:11310/11:10107123 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/11:9881 RIV/00216208:11130/11:7154 RIV/61989592:15110/11:10224809 RIV/00064203:_____/11:7154
Result on the web
<a href="http://dx.doi.org/10.1007/s12253-011-9385-8" target="_blank" >http://dx.doi.org/10.1007/s12253-011-9385-8</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s12253-011-9385-8" target="_blank" >10.1007/s12253-011-9385-8</a>
Alternative languages
Result language
angličtina
Original language name
Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas
Original language description
Pheochromocytomas (PCCs) are rare tumors among children and adolescents and therefore are not genetically well characterized. The most frequently observed chromosomal changes in PCC are losses of 1p, 3q and/or 3p, 6q, 17p, 11q, 22q, and gains of 9q and 17q. Aberrations involving chromosome 11 are more common in malignant tumors. Unfortunately information about gene aberrations in childhood PCC's is limited. We used comparative genomic hybridization (CGH) and array comparative genomic hybridization (aCGH) to screen for copy number changes in four children suffering from pheochromocytoma or paraganglioma. Patients were diagnosed at the age 13 or 14 years. Bilateral pheochromocytoma was associated with von Hippel-Lindau syndrome (VHL). Multiple paraganglioma was associated with a germline mutation in SDHB. We found very good concordance between the results of CGH and aCGH techniques. Losses were observed more frequently than gains. All cases had a loss of chromosome 11 or 11p. Other aberr
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Pathology Oncology Research
ISSN
1219-4956
e-ISSN
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Volume of the periodical
17
Issue of the periodical within the volume
4
Country of publishing house
GB - UNITED KINGDOM
Number of pages
8
Pages from-to
801-808
UT code for WoS article
000295588000003
EID of the result in the Scopus database
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