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Usherjev sindrom = Usher syndromeFakin, Ana ; Glavač, Damjan ; Hawlina, MarkoUsher syndrome is an autosomal recessive disease with prevalence of 3-6/100.000 and is the most common syndrome that affects vision and hearing. Three subtypes are distinguished on the basis of ... different degree of hearing loss. All patients develop retinitis pigmentosa with night vision difficultiesand constriction of visual field, and ultimately a decline in visual acuity and color vision. Future holds promise for gene therapy. We present a patient with typical clinical picture of Usher syndrome, who startednoticing night vision problems at age 13. At age 25 he was operated on for posterior cortical cataracts. At age 34 he has only 5-10° of visual field remaining with 1.0 visual acuity in both eyes. Fundus autofluorescence imagingrevealed a typical hyperautofluorescent ring on the border between normal and affected retina.Source: Zdravniški vestnik : glasilo Slovenskega zdravniškega društva = Slovenian medical journal = journal of Slovenian Medical Association. - ISSN 1318-0347 (Letn. 81, supl., jun. 2012, str. I-133-I-139)Type of material - article, component part ; adult, seriousPublish date - 2012Language - slovenianCOBISS.SI-ID - 295852
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source: Zdravniški vestnik : glasilo Slovenskega zdravniškega društva = Slovenian medical journal = journal of Slovenian Medical Association. - ISSN 1318-0347 (Letn. 81, supl., jun. 2012, str. I-133-I-139)
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Database name | Field | Year |
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Links to authors' personal bibliographies | Links to information on researchers in the SICRIS system |
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Fakin, Ana | 33340 |
Glavač, Damjan | 09275 |
Hawlina, Marko | 09154 |
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