Heitor Nogueira » Coats diasease

  • Coats disease

    Nov 8 2022 by Heitor Nogueira

    Fundus photograph of an 12-year-old asymptomatic patient. It is possible to observe the presence of vascular telangiectasias associated with areas of exudation without the presence of a tumor lesion.

    Photographer: Heitor Nogueira, Instituto Penido Burnier, Campinas-SP, Brazil

    Condition/keywords: Coats' disease


    Nov 8 2022 by Heitor Nogueira


    Photographer: Heitor Nogueira

    Condition/keywords: bear tracks, CHRPE, congenital hypertrophy of the retinal pigment epithelium (CHRPE)

  • Spontaneous lens dislocation (Weill Marchesani Syndrome)

    Nov 9 2022 by Heitor Nogueira

    A 9 year-old Male patient diagnosed with Weill Marchesani presented spontaneous bilateral lens dislocation. Weill-Marchesani syndrome, also known as spherophakia-brachymorphy syndrome and mesodermal dysmorphodystrophy, is an inherited connective tissue disorder characterized by eye lens abnormalities, secondary glaucoma, short stature, brachydactyly, joint stiffness, and cardiovascular defects.

    Photographer: Heitor Nogueira, Insituto Penido Burnier, Campinas-SP, Brazil

    Condition/keywords: mesodermal dysmorphodystrophy, spherophakia-brachymorphy syndrome, spontaneous lens dislocation, Weill Marchesani Syndrome