Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4006965 | Archivos de la Sociedad Española de Oftalmología | 2015 | 4 Pages |
Abstract
Marfan syndrome is a connective tissue disorder with autosomal dominant inheritance caused by fibrillin gene mutation. Ectopia lentis is the predominant ocular abnormality and a major diagnostic criterion. An association between Marfan syndrome and glaucoma has also been demonstrated. The reported case is unusual in that a complete spontaneous lens dislocation to vitreous was present and progressed to secondary lens particle open angle glaucoma.
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Authors
E. Arranz-Marquez, B. Fatela-Cantillo, M. Figueroa, M.Á. Teus,