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Related Concept Videos

The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The Retinoblastoma Gene01:20

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Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
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Diabetic Retinopathy

DefinitionDiabetic retinopathy is a microvascular complication of diabetes affecting the retinal blood vessels.Risk FactorsDiabetic retinopathy is present in almost all individuals with type 1 diabetes and more than 60% of those with type 2 diabetes after two decades of disease.The risk increases with poor glycemic control, hypertension, dyslipidemia, smoking, pregnancy, and puberty.Although cataracts and glaucoma are also more frequent in people with diabetes, retinopathy remains the leading...

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Related Experiment Video

Updated: Jun 7, 2026

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
06:15

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia

Published on: August 9, 2024

Septo-optic dysplasia.

M A Fard1, W Y Wu-Chen, B L Man

  • 1The Neuro-Ophthalmology Division, The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.

Pediatric Endocrinology Reviews : PER
|November 2, 2010
PubMed
Summary
This summary is machine-generated.

Septo-optic dysplasia is a rare condition affecting vision and brain development. Early, lifelong multidisciplinary care is vital for managing pituitary hormone deficiencies and developmental issues.

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Area of Science:

  • Pediatric Endocrinology
  • Neurodevelopmental Disorders
  • Ophthalmology

Background:

  • Septo-optic dysplasia (SOD) is a rare congenital disorder.
  • Characterized by optic nerve hypoplasia, midline brain defects, and pituitary hormone deficiencies.
  • Primarily sporadic, with rare familial occurrences.

Purpose of the Study:

  • To summarize the key features of Septo-optic dysplasia.
  • To highlight the clinical manifestations and management strategies.
  • To emphasize the importance of a multidisciplinary approach.

Main Methods:

  • Review of existing literature on Septo-optic dysplasia.
  • Analysis of characteristic clinical presentations.
  • Discussion of diagnostic criteria and management protocols.

Main Results:

  • Optic nerve hypoplasia impacts visual function.
  • Midline defects include agenesis of the septum pellucidum and corpus callosum abnormalities.
  • Pituitary hormone deficiencies require lifelong monitoring and treatment.

Conclusions:

  • Septo-optic dysplasia necessitates a comprehensive, lifelong management plan.
  • Multidisciplinary care optimizes growth and development for affected individuals.
  • Early intervention improves outcomes and quality of life.