2008
DOI: 10.1007/s10792-008-9264-9
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Fundus autofluorescence changes in two cases of Sjögren-Larsson syndrome

Abstract: Sjögren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder characterized by the triad of intellectual disability, spastic diplegia or tetraplegia, and congenital ichthyosis with associated ocular features, which include macular glistening dots. Herein, two cases of SLS are presented and their fundus autofluorescence changes, which have not been reported so far, are described.

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Cited by 3 publications
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“…Consequently aldehyde modified lipids or fatty alcohols accumulate, which are likely to disrupt the function of membranes in the eye, brain and skin. The deposits are fine, often hard to photograph, hyperautofluorescent and not associated with electrophysiological abnormality (Jagell et al, 1980;Mirshahi and Piri, 2009). …”
Section: Sjogren-larsson Syndrome (Sls)mentioning
confidence: 99%
“…Consequently aldehyde modified lipids or fatty alcohols accumulate, which are likely to disrupt the function of membranes in the eye, brain and skin. The deposits are fine, often hard to photograph, hyperautofluorescent and not associated with electrophysiological abnormality (Jagell et al, 1980;Mirshahi and Piri, 2009). …”
Section: Sjogren-larsson Syndrome (Sls)mentioning
confidence: 99%