ArticleIndian journal of ophthalmology2015
Prenatal genetic diagnosis of retinoblastoma--clinical correlates on follow-up.
Article in Indian journal of ophthalmology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
5 citing papers in PubMed, 11 citations in OpenAlex.
- Epidemiology, Diagnosis and Genetics of Retinoblastoma: ICMR Consensus Guidelines.Indian journal of pediatrics · 2024Review
- Prenatal Diagnosis of Retinoblastomas: A Scoping Review.International journal of general medicine · 2023Article
- Commentary: An eye on the genes.Indian journal of ophthalmology · 2022Article
- At What Age Could Screening for Familial Retinoblastoma Be Discontinued? A Systematic Review.Cancers · 2021Article
- Neonatal Retinoblastoma.Asia-Pacific journal of oncology nursingReview
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Retinoblastoma is the most common malignant intraocular tumor in pediatric age group if undetected leads to ocular mortality. Prenatal diagnosis is an emerging technology to detect fatal diseases in utero such that subsequent management is planned to reduce the ocular morbidity. We describe a case demonstrating the importance of prenatal diagnosis in a child with a strong family history of retinoblastoma and importance of a long-term clinical follow-up in these cases.
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Registered trials
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