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  Vol. 57 No. 3, March 1957 TABLE OF CONTENTS
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Ocular Myopathy Associated with Retinitis Pigmentosa

LT. COMDR. WAYNE L. ERDBRINK, MC

AMA Arch Ophthalmol. 1957;57(3):335-338.

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

Ocular myopathy is better known in the ophthalmic and neurologic literature as "chronic progressive nuclear ophthalmoplegia" or as "chronic progressive external ophthalmoplegia." The various terms stem from differences in opinion as to what constitutes the basic pathologic process. The older concept of nuclear origin in this entity1,2 was that of a degeneration of the nuclei of the oculomotor, trochlear, and abducens nerves. However, more recent pathologic studies3-6 indicate that this conclusion is not justified. Sorsby7 is of the opinion that ocular myopathy bears no relationship to motor neuron disease but is a form of muscular dystrophy. The pathologic data accumulated to date indicate that "chronic progressive external ophthalmoplegia" may rightly be considered as an "ocular myopathy," which is well summarized by Kiloh and Nevin.4

While uncommon, cases of progressive muscular dystrophy are reported in which the ocular muscles and muscles of the eye-lids have been involved. . . . [Full Text PDF of this Article]


Author Affiliations

U. S. N.

From the Ophthalmology Service, U. S. Naval Hospital, Philadelphia.


Footnotes

Received for publication Oct. 18, 1956.

The opinions or assertions contained herein are the private ones of the writer, and are not to be construed as official or reflecting the view of the Navy Department or the Naval Service at large.



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