Document Detail


Congenital blindness and osteoporosis-pseudoglioma syndrome.
MedLine Citation:
PMID:  12690376     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Isteoporosis-pseudoglioma syndrome (OPPG) is a rare heritable entity that features severe osteoporosis and many variable ophthalmic findings leading to congenital or juvenile blindness. These include microphthalmos, cataracts, bilateral pseudogliomatous retinal detachments, and phthisis bulbi. OPPG is usually not suspected until fractures occur, frequently after seemingly minor trauma. We report the ophthalmic findings of an infant girl with OPPG.
Authors:
Dave H Lee; Deborah Wenkert; Michael P Whyte; Michael T Trese; Oscar A Cruz
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus     Volume:  7     ISSN:  1091-8531     ISO Abbreviation:  J AAPOS     Publication Date:  2003 Feb 
Date Detail:
Created Date:  2003-04-11     Completed Date:  2003-10-29     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9710011     Medline TA:  J AAPOS     Country:  United States    
Other Details:
Languages:  eng     Pagination:  75-7     Citation Subset:  IM    
Affiliation:
St Louis University Eye Institute, St Louis, MO 63104, USA.
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MeSH Terms
Descriptor/Qualifier:
Arthrography
Blindness / complications*,  congenital*
Female
Femur / radiography
Glioma / complications*
Humans
Infant, Newborn
Knee Joint / radiography
Osteoporosis / complications*,  radiography
Syndrome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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