Source:http://linkedlifedata.com/resource/pubmed/id/17252279
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2007-5-3
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pubmed:abstractText |
Superficial hemosiderosis of the central nervous system (SH-CNS) is a relatively rare condition caused by chronic or repeated subarachnoid bleeding. The aim of this article was to present hearing disorders related to SH-CNS, and to describe results of magnetic resonance imaging (MRI) to confirm the diagnosis. We performed a retrospective case review at a tertiary referral center. Clinical presentation, auditory manifestations and MRI findings of two patients with SH-CNS are reported. The two patients experienced bilateral sensorineural hearing loss (SNHL) that progressively worsened. MRI revealed typical aspects of SH-CNS on T2-weighted images. Progressive bilateral SNHL is the most common manifestation of SH-CNS. The otolaryngologist should be aware of this disease that can be easily diagnosed with MRI.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0937-4477
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
264
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
701-4
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pubmed:meshHeading |
pubmed-meshheading:17252279-Adult,
pubmed-meshheading:17252279-Central Nervous System Diseases,
pubmed-meshheading:17252279-Diagnosis, Differential,
pubmed-meshheading:17252279-Female,
pubmed-meshheading:17252279-Hearing Aids,
pubmed-meshheading:17252279-Hearing Loss, Sensorineural,
pubmed-meshheading:17252279-Hemosiderosis,
pubmed-meshheading:17252279-Humans,
pubmed-meshheading:17252279-Magnetic Resonance Imaging,
pubmed-meshheading:17252279-Male
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pubmed:year |
2007
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pubmed:articleTitle |
Auditory manifestations of superficial hemosiderosis of the central nervous system.
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pubmed:affiliation |
Otology-Neurotology Unit, Department of Otolaryngology Head and Neck Surgery, Fondation Adolphe de Rothschild, 25-29 rue Manin, 75019, Paris, France. dayache@fo-rothschild.fr
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pubmed:publicationType |
Journal Article,
Case Reports
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