Document Detail


Familial foveal retinoschisis associated with a rod-cone dystrophy.
MedLine Citation:
PMID:  306756     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A brother and sister born of a consanguinous marriage had bilateral foveal retinoschisis and a generalized rod-cone dysfunction. This was associated with nyctalopia, hyperopia, minimal vitreous opacities in the sister, a paramacular tapetal sheen reflex, normal retinal vessels, an abnormal electroretinogram, and a normal electro-oculogram in the less affected brother. Foveal retinoschisis is not pathognomonic for x-chromosome-linked juvenile retinoschisis. It may be seen as a manifestation of a macular dystrophy or associated with a generalized tapetoretinal dystrophy.
Authors:
K G Noble; R E Carr; I M Siegel
Related Documents :
12689516 - Direct deletion analysis in two duchenne muscular dystrophy symptomatic females using p...
12062256 - Spinal muscular atrophy among the roma (gypsies) in bulgaria and hungary.
2801856 - Hereditary pigmented paravenous chorioretinal atrophy.
3029876 - A new probe for the diagnosis of myotonic muscular dystrophy.
16451666 - Critical values and variation in type i error along chromosomes in the coga dataset usi...
4111366 - Study of four new kindreds with inherited thyroxine-binding globulin abnormalities. pos...
Publication Detail:
Type:  Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  American journal of ophthalmology     Volume:  85     ISSN:  0002-9394     ISO Abbreviation:  Am. J. Ophthalmol.     Publication Date:  1978 Apr 
Date Detail:
Created Date:  1978-07-15     Completed Date:  1978-07-15     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  0370500     Medline TA:  Am J Ophthalmol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  551-7     Citation Subset:  AIM; IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adult
Child
Color Vision Defects / complications
Electroretinography
Female
Fluorescein Angiography
Fovea Centralis / pathology*
Humans
Macula Lutea / pathology*
Male
Night Blindness / complications
Photoreceptor Cells*
Reflex, Abnormal
Retinal Diseases / complications,  genetics*,  pathology
Vitreous Body / pathology

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


Previous Document:  Orbital apex syndrome secondary to herpes zoster ophthalmicus.
Next Document:  Specular microscopy of the corneal endothelium and lens implant surgery.