Definition: 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.
do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Other names Retinal Dysplasias; Dysplasias, Retinal; Dysplasia, Retinal
Substance
CAS Registry & name
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Source
Lymphedema, microcephaly and chorioretinopathy syndrome
