| Progressive visual loss in a child with Parry-Romberg syndrome. | |
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MedLine Citation:
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PMID: 15590544 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Progressive hemifacial atrophy in Parry-Romberg syndrome is associated with a wide variety of ophthalmologic findings. Progressive visual loss, especially in the first decade, is rare in this condition. We present a young girl originally felt to have linear scleroderma and anisometropic amblyopia, who was eventually diagnosed with Parry-Romberg syndrome as the cause of her cutaneous and ophthalmologic findings. |
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Authors:
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Thomas A Finley; R Michael Siatkowski |
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Publication Detail:
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Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Seminars in ophthalmology Volume: 19 ISSN: 0882-0538 ISO Abbreviation: Semin Ophthalmol Publication Date: 2004 Sep-Dec |
Date Detail:
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Created Date: 2004-12-13 Completed Date: 2005-03-07 Revised Date: 2008-05-28 |
Medline Journal Info:
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Nlm Unique ID: 8610759 Medline TA: Semin Ophthalmol Country: United States |
Other Details:
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Languages: eng Pagination: 91-4 Citation Subset: IM |
Affiliation:
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University of Oklahoma College of Medicine, Oklahoma City, Oklahoma, USA. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Cerebral Arteries
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pathology Child Disease Progression Facial Hemiatrophy / complications*, diagnosis, physiopathology Female Humans Magnetic Resonance Angiography Vision Disorders / diagnosis, etiology*, physiopathology |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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