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Pediatr Blood Cancer ; 54(3): 480-2, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19927293

RESUMEN

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.


Asunto(s)
Deleción Cromosómica , Cromosomas Humanos Par 13 , Anomalías del Ojo/genética , Retinoblastoma/genética , Femenino , Humanos , Lactante , Síndrome
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