Unilateral optic atrophy preceding Coats disease in a girl with Parry-Romberg syndrome.

Abstract:

PURPOSE:Parry-Romberg syndrome (PRS) is a rare disease of unknown etiology and pathogenesis, characterized by progressive hemifacial atrophy. Diverse ocular manifestations were reported in association with PRS, including enophthalmos, lid retraction, blepharoptosis, restrictive strabismus, ocular motor nerve dysfunction, Horner syndrome, reduced corneal sensitivity, band keratopathy, episcleritis, uveitis, neuroretinitis, and retinal vasculitis. METHODS:Descriptive case report. RESULT:We report on the development of unilateral optic atrophy followed by ipsilateral Coats disease exudation and shallow retinal detachment in the posterior pole and inferior retina. CONCLUSIONS:Optic atrophy was not previously described in association with PRS. We describe the development of unilateral optic atrophy with subsequent CD, 5 years later , in a girl with PRS.

journal_name

Eur J Ophthalmol

authors

Nasser O,Greiner K,Amer R

doi

10.1177/112067211002000132

subject

Has Abstract

pub_date

2010-01-01 00:00:00

pages

221-3

issue

1

eissn

1120-6721

issn

1724-6016

pii

AEDAC4E3-FAE4-4BC1-91E8-F44F02FD458C

journal_volume

20

pub_type

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