| Literature DB >> 651230 |
J P Gerhard, A Brini, D Willard, A Rohmer, J Messer.
Abstract
A Study is described of a family in which four children of the same generation died during early childhood; three of them had an obvious hydrocephalus. Two of the latter could be examined clinically, and their eyes removed for pathology. One of them presented clinically bilateral leucocoria; histology showed a total detachment of a dysplastic retina, with absence of development of the vitreous. The other child had apparently normal eyes. Yet on microscopical examination there was a discrete retinal dysplasia without retinal detachment in both eyes, and a persistent hyaloid artery, in one. This association of hydrocephalus with retinal dysplasia is clinically and genetically different from other types of retinal dysplasia.Entities:
Mesh:
Year: 1978 PMID: 651230
Source DB: PubMed Journal: Klin Monbl Augenheilkd ISSN: 0023-2165 Impact factor: 0.700