| Literature DB >> 24814393 |
Michael Dean1, Giovana Bendfeldt2, Hong Lou3, Veronica Giron4, Claudia Garrido4, Patricia Valverde4, Margarita Barnoya4, Mauricio Castellanos4, Silvia Jiménez-Morales5, Sandra Luna-Fineman6.
Abstract
Analysis of 327 consecutive cases at a pediatric referral hospital of Guatemala reveals that retinoblastoma accounts for 9.4% of all cancers and the estimated incidence is 7.0 cases/million children, higher than the United States or Europe. The number of familial cases is low, and there is a striking disparity in indigenous children due to late diagnosis, advanced disease, rapid progression and elevated mortality. Nine germline mutations in 18 patients were found; two known and five new mutations. Hypermethylation of RB1 was identified in 13% of the tumors. An early diagnosis program could identify cases at an earlier age and improve outcome of retinoblastoma in this diverse population. Published by Elsevier Ireland Ltd.Entities:
Keywords: Ethnicity; Guatemala; Health disparity; Methylation; Mutations; RB1 gene
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Year: 2014 PMID: 24814393 PMCID: PMC4490907 DOI: 10.1016/j.canlet.2014.04.023
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679