作者: M. Andrew Parsons , Diana Curtis , C. Eric Blank , Howard N. Hughes , Alison C. E. McCartney
DOI: 10.1007/BF00176299
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摘要: The ocular pathology of Norrie disease was studied for the first time in a fetus 11 weeks' gestation, following prenatal diagnosis using genetic markers and elective abortion. eyes were histologically normal, with no evidence primary neuroectodermal maldevelopment retina, previously postulated to be cause changes. We believe that retinal other manifestations are result abnormality vascular proliferation, probably relation persistent hyperplastic vitreous after approximately 14 gestation. postulate otological effects may due genetically mediated secretion of, or sensitivity to, angiogenic growth factors at endodermal-neuroectodermal interfaces during fetal postnatal development.