Retinal Dystrophy Diagnosed in a Biopsy and Gene Proven Neuronal Intranuclear Inclusion Disease Patient

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Identifier 20230312_nanos_posters_176
Title Retinal Dystrophy Diagnosed in a Biopsy and Gene Proven Neuronal Intranuclear Inclusion Disease Patient
Creator Chaoyi Feng; Qian Chen; Li Cao; Guohong Tian
Affiliation (CF) (QC) Department of Ophthalmology, Shanghai EENT; (LC) Department of Neurology, No.6 Hospital, Shanghai; (GT) Neuroophthalmology Division; Shanghai EENT Hospital
Subject Retina; Neuroimaging; Neuro-ophth & Systemic Disease (eg. MS, MG, Thyroid); Higher Visual Functions; Genetic Disease
Description Neuronal intranuclear inclusion disease (NIID) is a neurodegenerative disorder which is characterized by eosinophilic hyaline intranuclear inclusions found in central and peripheral nervous system and other tissues [1]. Retina dysfunctions as night blindness, retina dystrophy, and abnormal electroretinogram without blindness were only reported in several cases until now [2,3,4].
Date 2023-03-14
Language eng
Format application/pdf
Type Text
Source 2023 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS Annual Meeting 2023: Poster Session I: Neuro-Ophthalmic Disorders of Neurologic and Systemic Diseases
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Rights Management Copyright 2023. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6tj9w0g
Setname ehsl_novel_nam
ID 2335382
Reference URL https://collections.lib.utah.edu/ark:/87278/s6tj9w0g
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