Grönblad-Strandberg syndrome. Presentation of a patient

Authors

  • Zoila Fariñas Falcón Hospital Provincial Universitario “Arnaldo Milián Castro”, Santa Clara, Villa Clara
  • Rubén Antoliano Rangel Fleites Hospital Provincial Universitario “Arnaldo Milián Castro”, Santa Clara, Villa Clara
  • Amarilis Hernández Camacho Hospital Provincial Universitario “Arnaldo Milián Castro”, Santa Clara, Villa Clara

Keywords:

elasticum pseudoxanthoma

Abstract

Syndrome Grönblad-Strandberg is a rare hereditary disease it is a genetic disorder of connective tissue characterized by fragmentation of elastic fibers and subsequent calcification affecting the dermis, blood vessels and Bruch's membrane of retina. The inheritance pattern is highly variable, making it possible that this disease may be underdiagnosed. The low incidence of this condition justifies the presentation of a case who suffered decreased vision in both eyes by macular atrophy and causes of low vision.

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How to Cite

1.
Fariñas Falcón Z, Rangel Fleites RA, Hernández Camacho A. Grönblad-Strandberg syndrome. Presentation of a patient. Acta Méd Centro [Internet]. 2014 Jun. 28 [cited 2025 Jul. 12];8(2):102-6. Available from: https://revactamedicacentro.sld.cu/index.php/amc/article/view/134

Issue

Section

Case Reports