Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Searches for B^{0}→K^{+}π^{-}τ^{+}τ^{-} and B_{s}^{0}→K^{+}K^{-}τ^{+}τ^{-} Decays.

Physical review letters·2026
Same author

Precision Measurement of CP Violation and Branching Fractions in B^{±}→K_{S}^{0}h^{±} (h=π, K) Decays and Search for the Rare Decay B_{c}^{±}→K_{S}^{0}K^{±}.

Physical review letters·2026
Same author

First Observation of the B[over ¯]_{s}^{0}→Λ_{c}^{+}Λ[over ¯]_{c}^{-} Decay and Evidence for the B[over ¯]^{0}→Λ_{c}^{+}Λ[over ¯]_{c}^{-} Decay.

Physical review letters·2026
Same author

Observation of the Rare Baryonic Decay B^{+}→pΛ[over ¯] and Measurement of its Weak Decay Parameter.

Physical review letters·2026
Same author

Observation of B_{c}^{+}→Dh^{+}h^{-} Decays.

Physical review letters·2026
Same author

First Observation of CP Violation and Measurement of Polarization in B^{+}→ρ(770)^{0}K^{*}(892)^{+} Decays.

Physical review letters·2026

Related Experiment Video

Updated: Oct 29, 2025

Reconstruct Human Retinoblastoma In Vitro
06:52

Reconstruct Human Retinoblastoma In Vitro

Published on: October 11, 2022

1.5K

Retinoblastoma: A Major Review.

S R Roy1, S Kaliki

  • 1Dr Soma Rani Roy, Resident Surgeon, Chittagong Eye Infirmary and Training Complex, Bangladesh;

Mymensingh Medical Journal : MMJ
|July 6, 2021
PubMed
Summary
This summary is machine-generated.

Retinoblastoma, a common childhood eye cancer, requires early detection for better outcomes. Advances in treatment improve survival rates, but long-term follow-up is crucial for survivors due to secondary cancer risks.

More Related Videos

Establishment and Propagation of Human Retinoblastoma Tumors in Immune Deficient Mice
07:55

Establishment and Propagation of Human Retinoblastoma Tumors in Immune Deficient Mice

Published on: August 4, 2011

12.0K
Retinal Pigment Epithelium Transplantation in a Non-human Primate Model for Degenerative Retinal Diseases
11:20

Retinal Pigment Epithelium Transplantation in a Non-human Primate Model for Degenerative Retinal Diseases

Published on: June 14, 2021

4.0K

Related Experiment Videos

Last Updated: Oct 29, 2025

Reconstruct Human Retinoblastoma In Vitro
06:52

Reconstruct Human Retinoblastoma In Vitro

Published on: October 11, 2022

1.5K
Establishment and Propagation of Human Retinoblastoma Tumors in Immune Deficient Mice
07:55

Establishment and Propagation of Human Retinoblastoma Tumors in Immune Deficient Mice

Published on: August 4, 2011

12.0K
Retinal Pigment Epithelium Transplantation in a Non-human Primate Model for Degenerative Retinal Diseases
11:20

Retinal Pigment Epithelium Transplantation in a Non-human Primate Model for Degenerative Retinal Diseases

Published on: June 14, 2021

4.0K

Area of Science:

  • Ophthalmology
  • Pediatric Oncology
  • Genetics

Background:

  • Retinoblastoma is the most frequent primary intraocular tumor in children.
  • It affects 1 in 16,000–18,000 live births, representing 11% of infant cancers.
  • While often unilateral (60%), bilateral cases (40%) are heritable, with a median diagnosis age of 1 year.

Purpose of the Study:

  • To outline the diagnosis and treatment of retinoblastoma.
  • To emphasize the importance of early detection and multidisciplinary care.
  • To highlight the need for long-term follow-up and genetic counseling for survivors.

Main Methods:

  • Diagnosis relies on fundus examination, ultrasonography, and imaging (CT, MRI).
  • Treatment strategies are tailored to tumor laterality, size, location, and extent.
  • Genetic screening and counseling are vital for heritable forms.

Main Results:

  • Early detection and multidisciplinary treatment significantly improve prognosis.
  • Survival rates for retinoblastoma have increased due to treatment advancements.
  • Survivors face a risk of developing second cancers, necessitating long-term monitoring.

Conclusions:

  • Prompt diagnosis and comprehensive management are key to saving the child, globe, and vision.
  • Genetic factors, particularly RB1 gene mutations, play a role in heritable retinoblastoma.
  • Ongoing surveillance and genetic counseling are essential for retinoblastoma survivors and their families.