Papilledema from Pycnodysostosis

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Identifier 20120214_nanos_posters_038
Title Papilledema from Pycnodysostosis
Creator Kyung, Sungeun; Horton, Jonathan C
Subject Pycnodysostosis; craniosynostosis; Papilledema; cathepsin K
Description Pycnodysostosis is an autosomal recessive skeletal disorder caused by a mutation in the gene for cathepsin K, a lysosomal proteinase required for bone remodeling by osteoclasts. It is usually associated with delayed closure of the cranial sutures. Craniosynostosis is a rare manifestation of this condition.
Date 2012-02-14
Language eng
Format application/pdf
Format Creation application/pdf
Type Text
Source 2012 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 2012: Poster Presentations
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 2012. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s65q82ks
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 181862
Reference URL https://collections.lib.utah.edu/ark:/87278/s65q82ks
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