| Literature DB >> 19927293 |
Ana Roche1, Jaume Mora, Maria Del Mar Perez, Esther Gean, Belen Perez, Mar O'Callaghan, Jaume Catala, Carmen De Torres, Ofelia Cruz, Joan Prat, Andreu Parareda.
Abstract
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. Copyright 2009 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2010 PMID: 19927293 DOI: 10.1002/pbc.22354
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167