Diagnosed Case of Sjogren Larsson

file Retina Image Bank

File number: 60182


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    Appears in
    Miscellaneous
    Condition/keywords
    Sjogren's syndrome
    Photographer
    Ravikrishna, Puttaswamy
    Imaging device
    Optical coherence tomography system
    DRI OCT triton SSOCT-Topcon
    Description
    Hyperreflective deposits seen in inner plexiform layers. Sjogren Larsson is inborn error of lipid metabolism caused by mutation in FADH gene which leads to MCFA, LCFA build up specifically in the membranes of skin and brain. This picture shows shows deposits in IPL.

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