| A case of Sturge-Weber syndrome in association with phacomatosis pigmentovascularis and developmental glaucoma. | |
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MedLine Citation:
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PMID: 17512229 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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Sturge-Weber syndrome is a rare neurocutaneous disorder characterized by a facial nevus flammeus and extensive angiomatous changes involving the leptomeninges, the dura, and vessels of the gray and white matter. Oculodermal melanocytosis is characterized by hyperpigmentation of the facial skin in the distribution of the ophthalmic, maxillary, and occasionally mandibular division of the trigeminal nerve. |
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Authors:
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Archana Gupta; Suneeta Dubey; Manisha Agarwal |
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Publication Detail:
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Type: Journal Article Date: 2007-05-23 |
Journal Detail:
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Title: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus Volume: 11 ISSN: 1091-8531 ISO Abbreviation: J AAPOS Publication Date: 2007 Aug |
Date Detail:
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Created Date: 2007-08-10 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9710011 Medline TA: J AAPOS Country: United States |
Other Details:
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Languages: eng Pagination: 398-9 Citation Subset: IM |
Affiliation:
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Department of Paediatric Ophthalmology, Department of Glaucoma, Department of Vitreoretina, Dr. Shroff's Charity Eye Hospital, Daryaganj, New Delhi, India. archanaguptamahajan@gmail.com |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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