Primary photoreceptor degenerations: Terminology

M. E. Pennesi; P. J. Francis; R. G. Weleber

doi:10.1016/B978-0-12-374203-2.00209-8

Primary photoreceptor degenerations: Terminology

M. E. Pennesi, P. J. Francis, R. G. Weleber

Ophthalmology

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Abstract

Retinitis pigmentosa is caused by a large number of genetic defects that result in a characteristic pattern of degeneration of the rod and cone photoreceptors and the retinal pigment epithelium.

Original language	English (US)
Title of host publication	Encyclopedia of the Eye
Publisher	Elsevier
Pages	516-525
Number of pages	10
ISBN (Electronic)	9780123742032
ISBN (Print)	9780123741981
DOIs	https://doi.org/10.1016/B978-0-12-374203-2.00209-8
State	Published - Jan 1 2010

Keywords

Bardet-Biedl syndrome
Bone spicules
Cone dystrophy
Cone-rod dystrophy
Dark adaptation
ERG
Electroretinogram
Leber congenital amaurosis
Pigmentary retinopathy
Retinal degeneration
Retinal dystrophy
Retinitis pigmentosa
Rod-cone dystrophy
Syndromic retinitis pigmentosa
Usher syndrome
Visual fields

ASJC Scopus subject areas

General Medicine

Access to Document

10.1016/B978-0-12-374203-2.00209-8

Cite this

@inbook{c6cd6021619e4acc8f0c8be9917c81c6,

title = "Primary photoreceptor degenerations: Terminology",

abstract = "Retinitis pigmentosa is caused by a large number of genetic defects that result in a characteristic pattern of degeneration of the rod and cone photoreceptors and the retinal pigment epithelium.",

keywords = "Bardet-Biedl syndrome, Bone spicules, Cone dystrophy, Cone-rod dystrophy, Dark adaptation, ERG, Electroretinogram, Leber congenital amaurosis, Pigmentary retinopathy, Retinal degeneration, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Syndromic retinitis pigmentosa, Usher syndrome, Visual fields",

author = "Pennesi, {M. E.} and Francis, {P. J.} and Weleber, {R. G.}",

year = "2010",

month = jan,

day = "1",

doi = "10.1016/B978-0-12-374203-2.00209-8",

language = "English (US)",

isbn = "9780123741981",

pages = "516--525",

booktitle = "Encyclopedia of the Eye",

publisher = "Elsevier",

}

TY - CHAP

T1 - Primary photoreceptor degenerations

T2 - Terminology

AU - Pennesi, M. E.

AU - Francis, P. J.

AU - Weleber, R. G.

PY - 2010/1/1

Y1 - 2010/1/1

N2 - Retinitis pigmentosa is caused by a large number of genetic defects that result in a characteristic pattern of degeneration of the rod and cone photoreceptors and the retinal pigment epithelium.

AB - Retinitis pigmentosa is caused by a large number of genetic defects that result in a characteristic pattern of degeneration of the rod and cone photoreceptors and the retinal pigment epithelium.

KW - Bardet-Biedl syndrome

KW - Bone spicules

KW - Cone dystrophy

KW - Cone-rod dystrophy

KW - Dark adaptation

KW - ERG

KW - Electroretinogram

KW - Leber congenital amaurosis

KW - Pigmentary retinopathy

KW - Retinal degeneration

KW - Retinal dystrophy

KW - Retinitis pigmentosa

KW - Rod-cone dystrophy

KW - Syndromic retinitis pigmentosa

KW - Usher syndrome

KW - Visual fields

UR - http://www.scopus.com/inward/record.url?scp=85079827827&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85079827827&partnerID=8YFLogxK

U2 - 10.1016/B978-0-12-374203-2.00209-8

DO - 10.1016/B978-0-12-374203-2.00209-8

M3 - Chapter

AN - SCOPUS:85079827827

SN - 9780123741981

SP - 516

EP - 525

BT - Encyclopedia of the Eye

PB - Elsevier

ER -

Primary photoreceptor degenerations: Terminology

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this