| Vitreous veils and radial lattice in Marshall syndrome. | |
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MedLine Citation:
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PMID: 19005991 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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PURPOSE: To report the findings of membranous vitreous veils and radial lattice in a child with Marshall syndrome. DESIGN: Observational case report. METHODS: Retrospective review of medical records and fundus photograph of a 6-year-old boy with Marshall syndrome. RESULTS: Vitreoretinal findings were significant for bilateral membranous vitreous veils and radial lattice degeneration. CONCLUSIONS: This case demonstrates the occurrence of vitreous veils and radial lattice degeneration in patients with Marshall syndrome. |
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Authors:
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Jacob W Brubaker; Brian G Mohney; Jose S Pulido; Dusica Babovic-Vuksanovic |
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: Ophthalmic genetics Volume: 29 ISSN: 1744-5094 ISO Abbreviation: Ophthalmic Genet. Publication Date: 2008 Dec |
Date Detail:
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Created Date: 2008-11-13 Completed Date: 2008-11-18 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9436057 Medline TA: Ophthalmic Genet Country: England |
Other Details:
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Languages: eng Pagination: 184-5 Citation Subset: IM |
Affiliation:
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Department of Ophthalmology, University of Utah School of Medicine, Salt Lake City, Utah, USA. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Child Collagen Type XI / genetics Craniofacial Abnormalities / genetics* Eye Diseases / genetics* Hearing Loss, Sensorineural / genetics* Humans Male Osteochondrodysplasias / genetics* Point Mutation Retinal Degeneration / genetics* Retrospective Studies Syndrome Vitreous Body / pathology* |
| Chemical | |
Reg. No./Substance:
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0/Collagen Type XI |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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