Ocular Manifestations of Congenital/Inherited Diseases

Update item information
Identifier 94_17
Title Ocular Manifestations of Congenital/Inherited Diseases
Subject von Hippel-Lindau Disease
Description This 21-year-old woman had a 2-year history of blurred vision. A computerized visual field demonstrated a temporal defect OS. MRI confirmed a chiasmal mass lesion. The pathology was consistent with hemangioblastoma. Further workup revealed retinal angiomas and multiple other hemangioblastomas of the neural axis. CT scan of the abdomen demonstrated renal cysts. No other family members had von Hippel-Lindau disease. Disease/Diagnosis: von Hippel-Lindau Disease.
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 32, Part A
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 Steven Galetta, MD, NYU Langone Medical Center
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/s61g3kv1
Setname ehsl_novel_aao_nanos
Date Created 2004-11-17
Date Modified 2021-08-12
ID 176773
Reference URL https://collections.lib.utah.edu/ark:/87278/s61g3kv1
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