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  Vol. 70 No. 2, August 1963 TABLE OF CONTENTS
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Cone Dysfunction Syndromes

GEORGE GOODMAN, MD; HARRIS RIPPS, PhD; IRWIN M SIEGEL, PhD

Arch Ophthalmol. 1963;70(2):214-231.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Introduction

Cone dysfunction syndrome is the term used in the present investigation to designate a generalized disturbance of the cone system resulting in subnormal visual acuity, defective color vision, and absence of the photopic flicker electroretinogram; concomitant signs may include nystagmus and photophobia. The fundus is normal or may show a variety of lesions which cannot be considered pathognomonic of the condition. The bestknown form of the syndrome is congenital and is commonly referred to as total color blindness, monochromacy, or typical achromatopsia—terms which place emphasis upon the severe loss of color vision.

Although it is now apparent that the incidence of generalized cone pathology is much greater than previously assumed,1-3 a lack of awareness of the clinical symptomatology has resulted in frequent misdiagnoses. Many of the patients to be reported had earlier diagnoses of optic atrophy, macular degeneration, cerebral pathology, albinism, congenital nystagmus, or merely "unexplained amblyopia."

The . . . [Full Text PDF of this Article]


Author Affiliations

New York

From the Department of Ophthalmology, New York University School of Medicine.


Footnotes

Submitted for publication Feb 15, 1963.

This study was supported by a grant (B-2589) of the National Institute of Neurological Diseases and Blindness, National Institutes of Health.



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