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- W1436633191 abstract "Pediatric genetic ocular tumors include malignancies like retinoblastoma and phakomatosis like neurofibromatosis, tuberous sclerosis, von Hippel-Lindau syndrome, and nevoid basal cell carcinoma syndrome. It is important to screen for ocular tumors both for visual prognosis and also for systemic implications. The phakomatosis comprise of multitude of benign tumors that are aysmptomatic but their detection can aid in the diagnosis of the syndrome. Retinoblastoma is the most common malignant intraocular tumor in childhood and with current treatment modalities, the survival is more than 95%. It is transmitted as an autosomal dominant fashion and hence the offsprings of all patients with the germline retinoblastoma need to be screened from birth. This review discusses the various pediatric genetic ocular tumors discussing the clinical manifestation, diagnosis and treatment." @default.
- W1436633191 created "2016-06-24" @default.
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- W1436633191 date "2015-07-27" @default.
- W1436633191 modified "2023-09-24" @default.
- W1436633191 title "Pediatric genetic ocular tumors" @default.
- W1436633191 doi "https://doi.org/10.3233/pge-14107" @default.
- W1436633191 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5020998" @default.
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