| Literature DB >> 15926151 |
Suradej Hongeng1, Surapan Parapakpenjun, Samart Pakakasama, Busaba Rerkamnuaychoke, Ratanaporn Pornkul.
Abstract
We report a boy with constitutional deletion 13q chromosome associated with dysmorphic features and bilateral retinoblastoma. The patient developed secondary Burkitt lymphoma 5 years after the diagnosis of retinoblastoma at the age of 8 months. He has completed treatment for both malignancies. At present, he is 7 years old and still in remission.Entities:
Mesh:
Year: 2006 PMID: 15926151 DOI: 10.1002/pbc.20372
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167