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Visual and auditory anomalies in Chediak-Higashi syndrome

dc.contributor.authorCreel, Donnellen_US
dc.contributor.authorBoxer, Laurence A.en_US
dc.contributor.authorFauci, Anthony S.en_US
dc.date.accessioned2006-04-07T18:44:53Z
dc.date.available2006-04-07T18:44:53Z
dc.date.issued1983-03en_US
dc.identifier.citationCreel, Donnell, Boxer, Laurence A., Fauci, Anthony S. (1983/03)."Visual and auditory anomalies in Chediak-Higashi syndrome." Electroencephalography and Clinical Neurophysiology 55(3): 252-257. <http://hdl.handle.net/2027.42/25282>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6SYX-482YXFJ-9W/2/b677a6c2431981bf4a51c72c1cbaffbeen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25282
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6186456&dopt=citationen_US
dc.description.abstractAlbinism is correlated with misrouting of decussating retinal fibers in the brain. There is also evidence of anomalies of decussating auditory pathways in albinos. The Chediak-Higashi syndrome (CHS) is a rare form of partial albinism which includes increased susceptibility to infections, a hemorrhagic tendency and peripheral polyneuropathies. Binocular and monocular pattern-onset visually evoked potentials (VEPs) and monaural auditory brain stem responses (ABRs) were recorded from 4 subjects with CHS. Three of the CHS demonstrated asymmetric monocular VEPs and failed the Titmus stereovision test. All 4 CHS produced asymmetric ABRs similar to those reported for albinos. Although the hair, skin and irises are relatively well pigmented in CHS, these individuals apparently have anomalies of their central visual and auditory pathways.en_US
dc.format.extent426420 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleVisual and auditory anomalies in Chediak-Higashi syndromeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatric Hematology, School of Medicine, University of Michigan, Ann Arbor, Mich. 48109, U.S.A.en_US
dc.contributor.affiliationotherVeterans Administration Medical Center, and Department of Ophthalmology, University of Utah, Salt Lake City, Utah 84148, U.S.A.en_US
dc.contributor.affiliationotherNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md. 20205, U.S.A.en_US
dc.identifier.pmid6186456en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25282/1/0000725.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0013-4694(83)90202-Xen_US
dc.identifier.sourceElectroencephalography and Clinical Neurophysiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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