A complex karyotype in an atypical teratoid/rhabdoid tumor: case report and review of the literature

Atypical teratoid/rhabdoid tumor (AT/RT) is a highly aggressive and uncommon neoplasm of the central nervous system that usually occurs in children less than 2 years of age. It is characterized by deletions and/or mutations of the INI1 tumor suppressor gene located in chromosome band 22q11.2. We per...

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Veröffentlicht in:	Journal of neuro-oncology 2011-08, Vol.104 (1), p.375-380
Hauptverfasser:	Coccé, Mariela C., Lubieniecki, Fabiana, Kordes, Uwe, Alderete, Daniel, Gallego, Marta S.
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Case Report Case reports Central nervous system Children Chromosomal Proteins, Non-Histone - genetics Chromosome Deletion Chromosomes, Human, Pair 22 - genetics DNA-Binding Proteins - genetics epigenetics Evolution Evolutionary genetics Gene deletion Genomes Genomic instability Humans Infant INI1 protein Karyotypes Karyotyping - methods Literature reviews Male Medicine Medicine & Public Health Monosomy Mutation Mutation - genetics Neurology Oncology Polyploidy Reviews Rhabdoid Tumor - diagnosis Rhabdoid Tumor - genetics SMARCB1 Protein Teratoma - diagnosis Teratoma - genetics Transcription Factors - genetics Tumor suppressor genes Tumors
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