Cogan’s syndrome

Rex M. McCallum; E. William St Clair; Barton F. Haynes

doi:10.1201/b14012

Cogan’s syndrome

Rex M. McCallum, E. William St Clair, Barton F. Haynes

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

1 Scopus citations

Abstract

The hallmarks of Cogan’s syndrome (CS) are interstitial keratitis (IK) and vestibuloauditory dysfunction. The history of CS reflects a growing awareness of its potential for causing not only eye and ear disease, but also complex systemic manifestations. In 1945, David G. Cogan, an ophthalmologist at the Harvard Medical School, reported four cases of recurrent nonsyphilitic IK and vestibuloauditory symptoms (1). These cases were similar to a patient who had been described in 1934 with IK and Meniere’s disease (2). Cogan was later credited with the first description of this disorder, which now bears his name (1).

Original language	English (US)
Title of host publication	Inflammatory Diseases of Blood Vessels
Publisher	CRC Press
Pages	491-509
Number of pages	19
ISBN (Electronic)	9780824746599
ISBN (Print)	9780824703844
DOIs	https://doi.org/10.1201/b14012
State	Published - Jan 1 2000
Externally published	Yes

ASJC Scopus subject areas

General Medicine

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title = "Cogan{\textquoteright}s syndrome",

abstract = "The hallmarks of Cogan{\textquoteright}s syndrome (CS) are interstitial keratitis (IK) and vestibuloauditory dysfunction. The history of CS reflects a growing awareness of its potential for causing not only eye and ear disease, but also complex systemic manifestations. In 1945, David G. Cogan, an ophthalmologist at the Harvard Medical School, reported four cases of recurrent nonsyphilitic IK and vestibuloauditory symptoms (1). These cases were similar to a patient who had been described in 1934 with IK and Meniere{\textquoteright}s disease (2). Cogan was later credited with the first description of this disorder, which now bears his name (1).",

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AB - The hallmarks of Cogan’s syndrome (CS) are interstitial keratitis (IK) and vestibuloauditory dysfunction. The history of CS reflects a growing awareness of its potential for causing not only eye and ear disease, but also complex systemic manifestations. In 1945, David G. Cogan, an ophthalmologist at the Harvard Medical School, reported four cases of recurrent nonsyphilitic IK and vestibuloauditory symptoms (1). These cases were similar to a patient who had been described in 1934 with IK and Meniere’s disease (2). Cogan was later credited with the first description of this disorder, which now bears his name (1).

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Cogan’s syndrome

Abstract

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