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Pediatr Blood Cancer ; 54(3): 480-2, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19927293

RESUMO

Axenfeld-Rieger (AR) ocular anomaly might be due to deletions of different chromosomes. No association between AR, mental retardation, and retinoblastoma has been described. We report a 2-month-old female with general development delay and dysmorphic features. AR anomaly was detected, and a retinoblastoma (RB) was diagnosed in a very early stage. De novo 13q deletion was identified. Systemic chemotherapy, focal cryotherapy, transpupillary thermotherapy, brachytherapy, and intra-arterial chemotherapy were needed to control the RB. This is the first report of an association of AR, 13q deletion, and retinoblastoma, to be disclosed in patients born with such ocular and dysmorphic features.


Assuntos
Deleção Cromossômica , Cromossomos Humanos Par 13 , Anormalidades do Olho/genética , Retinoblastoma/genética , Feminino , Humanos , Lactente , Síndrome
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