Elad Moisseiev, MD » Miscellaneous

  • Bear Tracks

    Dec 27 2016 by Elad Moisseiev, MD

    A 34-year-old man with bear tracks noted on routine exam. There was no personal or family history of Gardner syndrome or any GI malignancy.

    Photographer: Galit Yair-Pur

    Condition/keywords: bear tracks

  • Best Macular Dystrophy

    Dec 27 2016 by Elad Moisseiev, MD

    A 38-year-old male patient with complaints of central vision decrease – for 10 years. Fundus: macular atrophic changes, yellowish macular deposits with a paracentral macular yellow ring. Genetics: A heterozygous mutation in Best1 gene - c.874G>A ; p.E292K was found, confirming the diagnosis of Best macular dystrophy.

    Photographer: Galit Yair-Pur

    Condition/keywords: Best disease

  • Cat Scratch Disease

    Dec 27 2016 by Elad Moisseiev, MD

    A 31-year-old man with cat scratch disease (positive serology for Bartonella hensleae), which resulted in a 2 nasal branch retinal artery occlusions associated with a temporal visual field defect.

    Photographer: Gailt Yair-Pur

    Condition/keywords: branch retinal artery occlusion (BRAO), cat scratch retinitis

  • Combined Retinal Artery and Vein Occlusion

    Dec 27 2016 by Elad Moisseiev, MD

    A 51-year-old man with combined branch retinal artery and vein occlusion.

    Photographer: Galit Yair-Pur

    Condition/keywords: branch retinal artery occlusion (BRAO), branch retinal vein occlusion (BRVO)

  • Familial Exudative Vitreoretinopathy

    Dec 27 2016 by Elad Moisseiev, MD

    A 14-year-old girl with FEVR. In her left eye shown here there was a long standing exudative retinal detachment with reduced visual acuity.

    Photographer: Galit Yair-Pur

    Condition/keywords: familial exudative vitreoretinopathy (FEVR)

  • Fundus Albipunctata

    Dec 27 2016 by Elad Moisseiev, MD

    A 53-year-old female patient with high myopia and complaints of stationary night blindness since childhood. Fundus: myopic fundus with yellow dots in the posterior pole. Genetics: Homozygous mutations in RDH5 gene - c.160C>T (p.R54X), confirming the diagnosis of fundus albipunctata.

    Photographer: Galit Yair-Pur

    Condition/keywords: fundus albipunctatus

  • Peripheral Lattice Degeneration

    Dec 27 2016 by Elad Moisseiev, MD

    An asymptomatic 14 year old girl with peripheral lattice noted on routine exam.

    Photographer: Galit Yair-Pur

    Condition/keywords: peripheral lattice degeneration

  • Retinitis Pigmentosa

    Dec 27 2016 by Elad Moisseiev, MD

    A 65-year-old woman with end stage retinitis pigmentosa (HM vision).

    Photographer: Galit Yair-Pur

    Condition/keywords: retinitis pigmentosa