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  Vol. 59 No. 6, June 1958 TABLE OF CONTENTS
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Atypical Retinitis Pigmentosa, Acanthrocytosis, and Heredodegenerative Neuromuscular Disease

ROBERT S. JAMPEL, M.D.; HAROLD F. FALLS, M.D.

AMA Arch Ophthalmol. 1958;59(6):818-820.

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

The paper of Kornzweig and Bassen published in the A. M. A. ARCHIVES OF OPHTHALMOLOGY in August, 1957, "Retinitis Pigmentosa, Acanthrocytosis, and Heredodegenerative Neuromuscular Diseases," is of current interest. This intriguing combination of abnormalities has been reported to date in only three patients, the two pationts of Kornzweig and Bassen and the one of Singer, Fisher, and Perlstein. The patient of Singer et al., as known to Kornzweig and Bassen, exhibited the entire complex except for the retinitis pigmentosa. This patient, the son of first cousins, developed celiac disease at about the age of one year which was controlled by low-fat diet. At the age of 9 years acanthrocystosis was discovered, and at the age of 10 the insidious onset and slow progression of ataxia, intention tremor, athetoid movements, and impaired proprioceptive sense was noted.

It is the purpose of this paper to report a follow-up examination of the patient . . . [Full Text PDF of this Article]


Author Affiliations

Ann Arbor, Mich.

Instructor in Neurology (Dr. Jampel) and Associate Professor of Ophthalmology (Dr. Falls), University Hospital.


Footnotes

Received for publication Sept. 25, 1957.



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