
Congenital Hereditary Ptosis With Inferior Rectus FibrosisReport of Two Cases
Gunter K. von Noorden, MD
Arch Ophthalmol. 1970;83(3):378-380.
Abstract
A dominantly inherited disorder occurring in father and daughter consisted of unilateral ptosis and inability to elevate the depressed left eye. Abduction and adduction were normal on the affected side. Surgical exploration in one case revealed massive adhesions between the interior rectus muscles and adjacent tissues.
Author Affiliations
Baltimore
From the Wilmer Institute of Ophthalmology, The Johns Hopkins University School of Medicine and Hospital, Baltimore.
Footnotes
Submitted for publication July 2, 1969.
Reprint requests to the Wilmer Institute of Ophthalmology, The Johns Hopkins Hospital, Baltimore 21205 (Dr. von Noorden).
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