Osteopetrosis - A Rare Disease: A New Treatment

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Identifier 19900208_nanos_orbitsympos_07
Title Osteopetrosis - A Rare Disease: A New Treatment
Creator Jonathan D. Wirtschafter, MD
Affiliation University of Minnesota, Minneapolis, MN
Subject Osteopetrosis; Visual Loss; Anemia; Hepatosplenomegally; Extramedullary Hematopoesis; Compressive Optic Atrophy; Hydrocephalus; Papilledema; Infantile Amaurosis
Description Osteopetrosis describes a group of at least 8 inherited disorders of reduced osteoclast function that results in failure of bone resorption and a generalized increase in bone density. In some of these disorders there is an abnormality in bone marrow stem cells that affects osteoclasts and macrophages. Abnormalities of macrophages and neutophil activation partially explain the high susceptibility to infection. In other disorders abnormal osteoclast function may result from local environmental products that Influence cellular differentiation or regulation.
Date 1990-02-08
Language eng
Format application/pdf
Format Creation application/pdf
Type Text
Source 1990 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 1990: Orbit Symposium
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 2010. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6ng7x8n
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 183089
Reference URL https://collections.lib.utah.edu/ark:/87278/s6ng7x8n
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