Search results (2 results)

Jul 18 2025 by Kimberly Wakester

Optomap RGB and AF of an 63-year-old man with secondary pigmentary degeneration of the retina. Patient's Spark genetic testing revealed heterozygous mutations of unknown significance in LRP5, COL18A1, CPLANE1, SLC24A1 and VCAN. Clinical findings most consistent with Wagner's Syndrome (VCAN mutation, autosomal dominant). Will continue follow up care every 6 months with dilated exam and repeat OCT and Optos imaging.

Photographer: Kimberly Wakester, COA, OCT-C

Imaging device: Optos California

Condition/keywords: secondary pigmentary degeneration, Wagner's Syndrome

Jul 18 2025 by Kimberly Wakester

Optomap RGB and AF of an 63-year-old man with secondary pigmentary degeneration of the retina. Patient's Spark genetic testing revealed heterozygous mutations of unknown significance in LRP5, COL18A1, CPLANE1, SLC24A1 and VCAN. Clinical findings most consistent with Wagner's Syndrome (VCAN mutation, autosomal dominant). Will continue follow up care every 6 months with dilated exam and repeat OCT and Optos imaging .

Photographer: Kimberly Wakester, COA, OCT-C

Imaging device: Optos California

Condition/keywords: secondary pigmentary degeneration, Wagner disease