Leber's Hereditary Optic Neuropathy in Women

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Identifier 20210222_nanos_sciplatform2_04-video
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 Carell
Subject Genetic Disease; Neuro-ophth & 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.
Relation is Part of NANOS Annual Meeting 2021: Scientific Platform Session II
Contributor Primary Giulia Amore, MD
Contributor Secondary Martina Romagnoli, Chiara La Morgia, Michele Carbonelli, Francesca Allegrini, Rustum Karanjia, Alfredo Sadun, Valerio Carell
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2021-02
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Type Image/MovingImage
Format video/mp4
Source 2021 North American Neuro-Ophthalmology Society Annual Meeting
Rights Management Copyright 2021. 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
Language eng
ARK ark:/87278/s6sr4zp9
Setname ehsl_novel_nam
ID 1697223
Reference URL https://collections.lib.utah.edu/ark:/87278/s6sr4zp9
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