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 |