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
CAS Registry & name
Lymphedema, microcephaly and chorioretinopathy syndrome