Retinal Dysplasia

Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.

Year introduced: 1990

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C11.250.666, C11.270.660, C11.768.660, C16.131.384.784, C16.320.290.660

MeSH Unique ID: D015792

Entry Terms:

• Dysplasia, Retinal
• Dysplasias, Retinal
• Retinal Dysplasias

Previous Indexing:

• Retina/abnormalities (1966-1989)
• Retinal Degeneration (1970-1989)

All MeSH Categories
Diseases Category
Eye Diseases
Eye Abnormalities
Retinal Dysplasia

All MeSH Categories
Diseases Category
Eye Diseases
Eye Diseases, Hereditary
Retinal Dysplasia

All MeSH Categories
Diseases Category
Eye Diseases
Retinal Diseases
Retinal Dysplasia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Retinal Dysplasia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinal Dysplasia