Papilledema: initial sign of an INF2 mutation

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Identifier 20190317_nanos_posters_040
Title Papilledema: initial sign of an INF2 mutation
Creator David Rastall; David Kaufman; Lina Nagia; Kemar Green; Patrick O'Connell
Affiliation (DR) (DK) (LN) (KG) (PO) Michigan State University, East Lansing, Michigan
Subject Pseudotumor Cerebri; Genetic Disease
Description Idiopathic Intracranial Hypertension (IIH) is the most common cause of papilledema in young women, however; ~93% of patients have a BMI>25 (3) - IIH patients with low BMI should warrant a more robust clinical work-up.
Date 2019-03
Language eng
Format application/pdf
Type Text
Source 2019 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NAM 2019: Poster Session I: Clinical Highlights in Neuro-Ophthalmology
Collection Neuro-Ophthalmology Virtual Education Library: NANOS Annual Meeting Collection: https://novel.utah.edu/collection/nanos-annual-meeting-collection/
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2019. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6w99tm3
Setname ehsl_novel_nam
ID 1432227
Reference URL https://collections.lib.utah.edu/ark:/87278/s6w99tm3
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