Papilledema from Pycnodysostosis

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Identifier 20120214_nanos_posters_038
Title Papilledema from Pycnodysostosis
Creator Sungeun Kyung; Jonathan C. Horton
Affiliation (SK) Dankook University, Cheonan City, Republic of Korea; (JCH) University of California - San Francisco, San Francisco, CA
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
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: 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 2012. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s65q82ks
Setname ehsl_novel_nam
ID 181862
Reference URL https://collections.lib.utah.edu/ark:/87278/s65q82ks
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