Leber's Hereditary Optic Neuropathy in Women

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Identifier 20210222_nanos_sciplatform2_04-abstract
Title Leber's Hereditary Optic Neuropathy in Women
Creator Giulia Amore; Martina Romagnoli; Chiara La Morgia; Michele Carbonelli; Francesca Allegrini; Rustum Karanjia; Alfredo Sadun; Valerio Carelli
Affiliation (GA) (VC) Università di Bologna, Bologna, Italy; (MR) (CL) (MC) IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; (FA) University of Verona, Verona, Italy; (RK) University of Ottawa; Ottawa Hospital Research Institute, Ottawa, Canada; (AS) Doheny Eye Centers at UCLA; Doheny Eye Institute, Los Angeles, California
Subject Genetic Disease; Neuro-ophthalmology & Systemic Disease (eg. MS, MG, Thyroid); Optic Neuropathy
Description Leber's hereditary optic neuropathy (LHON) is a mitochondrial disorder characterized by selective degeneration of retinal ganglion cells with significant gender bias and incomplete penetrance. We aimed at refining the characteristics of LHON in women.
Date 2021-02
Language eng
Format application/pdf
Type Text
Source 2021 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS Annual Meeting 2021: Scientific Platform Session II
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 2021. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6t78cg7
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 1671208
Reference URL https://collections.lib.utah.edu/ark:/87278/s6t78cg7
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