Chorioretinal coloboma

Sally S. Ong

doi:10.1016/B978-0-323-60984-5.00055-X

Chorioretinal coloboma

Sally S. Ong

School of Medicine

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

Abstract

In chorioretinal colobomas, the sclera is staphylomatous, the overlying retina is atrophic, and the retinal pigment epithelium (RPE), Bruch membrane, choriocapillaries, and choroid can be absent and replaced by glial tissue. In this chapter, we discuss the clinical features, OCT features, ancillary testing, and treatment of children with chorioretinal coloboma.

Original language	English (US)
Title of host publication	Handbook of Pediatric Retinal OCT and the Eye-Brain Connection
Publisher	Elsevier
Pages	256-260
Number of pages	5
ISBN (Electronic)	9780323609845
ISBN (Print)	9780323609852
DOIs	https://doi.org/10.1016/B978-0-323-60984-5.00055-X
State	Published - Jan 1 2019

Keywords

CHARGE
Chorioretinal
Choroidal neovascular membrane
Coloboma
Retinal detachment

ASJC Scopus subject areas

Medicine(all)

Access to Document

10.1016/B978-0-323-60984-5.00055-X

Cite this

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title = "Chorioretinal coloboma",

abstract = "In chorioretinal colobomas, the sclera is staphylomatous, the overlying retina is atrophic, and the retinal pigment epithelium (RPE), Bruch membrane, choriocapillaries, and choroid can be absent and replaced by glial tissue. In this chapter, we discuss the clinical features, OCT features, ancillary testing, and treatment of children with chorioretinal coloboma.",

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AU - Ong, Sally S.

PY - 2019/1/1

Y1 - 2019/1/1

N2 - In chorioretinal colobomas, the sclera is staphylomatous, the overlying retina is atrophic, and the retinal pigment epithelium (RPE), Bruch membrane, choriocapillaries, and choroid can be absent and replaced by glial tissue. In this chapter, we discuss the clinical features, OCT features, ancillary testing, and treatment of children with chorioretinal coloboma.

AB - In chorioretinal colobomas, the sclera is staphylomatous, the overlying retina is atrophic, and the retinal pigment epithelium (RPE), Bruch membrane, choriocapillaries, and choroid can be absent and replaced by glial tissue. In this chapter, we discuss the clinical features, OCT features, ancillary testing, and treatment of children with chorioretinal coloboma.

KW - CHARGE

KW - Chorioretinal

KW - Choroidal neovascular membrane

KW - Coloboma

KW - Retinal detachment

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U2 - 10.1016/B978-0-323-60984-5.00055-X

DO - 10.1016/B978-0-323-60984-5.00055-X

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SN - 9780323609852

SP - 256

EP - 260

BT - Handbook of Pediatric Retinal OCT and the Eye-Brain Connection

PB - Elsevier

ER -

Chorioretinal coloboma

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

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