Document Detail


Bilateral retinal vascular hypoplasia associated with persistence of the primary vitreous: a new clinical entity?
MedLine Citation:
PMID:  3282058     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Three infant boys with a bilateral congenital retinopathy characterized by retinal vascular hypoplasia and persistence of the primary vitreous are described. The infants were healthy and had no non-ocular physical abnormalities. None had histories of prematurity or low birth weight. Family histories were negative to similar retinopathy, and the fundi of all examined blood relatives were normal. The described congenital retinopathy is compared and contrasted with persistent hyperplastic primary vitreous, Norrie's disease, idiopathic retinal dysplasia, familial exudative vitreoretinopathy, retinopathy of prematurity, and incontinentia pigmenti.
Authors:
P J Sneed; J J Augsburger; J A Shields; W Tasman; R Addiego
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of pediatric ophthalmology and strabismus     Volume:  25     ISSN:  0191-3913     ISO Abbreviation:  J Pediatr Ophthalmol Strabismus     Publication Date:    1988 Mar-Apr
Date Detail:
Created Date:  1988-05-26     Completed Date:  1988-05-26     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7901143     Medline TA:  J Pediatr Ophthalmol Strabismus     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  77-85     Citation Subset:  IM    
Affiliation:
Oncology Service, Wills Eye Hospital, Philadelphia, Pennsylvania 19107.
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MeSH Terms
Descriptor/Qualifier:
Electroretinography
Eye Diseases / complications,  diagnosis,  genetics,  pathology
Fluorescein Angiography
Follow-Up Studies
Fundus Oculi
Humans
Hydrophthalmos / complications
Infant
Male
Medical Records
Physical Examination
Retinal Vessels / abnormalities*
Ultrasonography
Vitreous Body*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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