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Pediatr Blood Cancer ; 46(4): 524-6, 2006 Apr.
Article in English | MEDLINE | ID: mdl-15926151

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.


Subject(s)
Burkitt Lymphoma/genetics , Chromosome Deletion , Chromosomes, Human, Pair 13/genetics , Neoplasms, Second Primary/genetics , Retinoblastoma/genetics , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Burkitt Lymphoma/diagnosis , Burkitt Lymphoma/drug therapy , Diagnosis, Differential , Humans , Infant , Male , Neoplasms, Second Primary/diagnosis , Neoplasms, Second Primary/drug therapy , Remission Induction , Retinoblastoma/diagnosis , Retinoblastoma/drug therapy , Syndrome , Treatment Outcome
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