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Ultra-high resolution 1M array CGH analysis detects no formerly unknown aberration of 17q unaltered neuroblastomas

A Hombach, J Theißen, R Spitz, B Hero, A Oberthuer, M Fischer, F Berthold · Klinische Pädiatrie · 2010 · Heft 05

Dokument
1015527
CareLit-ID
Jahr
2010
Publikation
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Pädiatrie
Autor:innen
A Hombach, J Theißen, R Spitz, B Hero, A Oberthuer, M Fischer, F Berthold
Ausgabe
Heft 05 / 2010
Seiten
–
Erschienen: 2010-05-07 00:00:00
ISSN
0300-8630

Zusammenfassung

Background: Additional chromosomal material on the long arm of chromosome 17 (17q gain) is present in the vast majority of neuroblastomas (NB). Therefore it has been discussed as a first hit in the pathogenesis. In a previous aCGH analysis of 202 NB patients with a resolution of up to 15kb, we found a small group of patients (7%) without alterations of 17q, but with a poor prognosis. We now reinvestigated this subgroup with ultra-high-resolution arrays. Methods: Twelve tumors were analyzed by 1M aCGH with a median resolution of 2kb. Aberrations of 1p and MYCN were additionally analyzed by FISH. Ten tumors were a…

Schlagworte

Klinische Pädiatrie