Pseudo oculomotor palsy as the presenting sign of linear scleroderma

Rosa A. Tang; L. Mewis-Christmann; J. Wolf; R. B. Wilkins

Pseudo oculomotor palsy as the presenting sign of linear scleroderma

Rosa A. Tang, L. Mewis-Christmann, J. Wolf, R. B. Wilkins

Research output: Contribution to journal › Article › peer-review

Abstract

A case of linear scleroderma presenting as a pseudo oculomotor palsy is reviewed. The patient's facial skin abnormalities suggested the underlying etiology. This case illustrates a previously unreported finding in linear scleroderma, mydriasis without atrophy, reminding the clinician to look at the skin in patients with unexplained unilateral pupillary disturbances.

Original language	English (US)
Pages (from-to)	236-238
Number of pages	3
Journal	Journal of Pediatric Ophthalmology and Strabismus
Volume	23
Issue number	5
State	Published - Jan 1 1986

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Ophthalmology

Cite this

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title = "Pseudo oculomotor palsy as the presenting sign of linear scleroderma",

abstract = "A case of linear scleroderma presenting as a pseudo oculomotor palsy is reviewed. The patient's facial skin abnormalities suggested the underlying etiology. This case illustrates a previously unreported finding in linear scleroderma, mydriasis without atrophy, reminding the clinician to look at the skin in patients with unexplained unilateral pupillary disturbances.",

author = "Tang, {Rosa A.} and L. Mewis-Christmann and J. Wolf and Wilkins, {R. B.}",

year = "1986",

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T1 - Pseudo oculomotor palsy as the presenting sign of linear scleroderma

AU - Tang, Rosa A.

AU - Mewis-Christmann, L.

AU - Wolf, J.

AU - Wilkins, R. B.

PY - 1986/1/1

Y1 - 1986/1/1

N2 - A case of linear scleroderma presenting as a pseudo oculomotor palsy is reviewed. The patient's facial skin abnormalities suggested the underlying etiology. This case illustrates a previously unreported finding in linear scleroderma, mydriasis without atrophy, reminding the clinician to look at the skin in patients with unexplained unilateral pupillary disturbances.

AB - A case of linear scleroderma presenting as a pseudo oculomotor palsy is reviewed. The patient's facial skin abnormalities suggested the underlying etiology. This case illustrates a previously unreported finding in linear scleroderma, mydriasis without atrophy, reminding the clinician to look at the skin in patients with unexplained unilateral pupillary disturbances.

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Pseudo oculomotor palsy as the presenting sign of linear scleroderma

Abstract

ASJC Scopus subject areas

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