Ocular Manifestations of Congenital/Inherited Diseases

Update item information
Identifier 94_23
Title Ocular Manifestations of Congenital/Inherited Diseases
Subject Wyburn-Mason Syndrome
Description This 38-year-old man had unexplained poor vision in his left eye all his life and was told that he had some type of congenital vascular anomaly. He had no neurocutaneous problems. The photographs demonstrate a complex arteriovenous malformation with dilated loops of veins extending out from the nerve head into the periphery and heading back toward the disc. Also note the direct vascular channels connecting arterioles to venules. MRI demonstrated a vascular malformation in the left suprasellar cistern. Disease/Diagnosis: Wyburn-Mason Syndrome.
Creator AAO/NANOS - American Academy of Ophthalmology / North American Neuro-Ophthalmology Society
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Type Image
Format image/jpeg
Relation is Part of Case 31
Rights Management Copyright 2002. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Contributor Primary Daniel M. Jacobson MD, Departments of Neurosciences and Ophthalmology, Marshfield Clinic, Marshfield, Wisconsin
Source AAO/NANOS Clinical neuro-ophthalmology : image collection for ophthalmic practitioners. American Academy of Ophthalmology [electronic resource], [San Francisco, Calif.] : AAO, c1999.
ARK ark:/87278/s6hf0v8k
Setname ehsl_novel_aao_nanos
Date Created 2004-11-17
Date Modified 2021-08-12
ID 176777
Reference URL https://collections.lib.utah.edu/ark:/87278/s6hf0v8k
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