Literature DB >> 19743786

Weill Marchesani syndrome with chronic angle closure glaucoma in Ethiopia: a case report.

Addis Tenkir1, Sisay Bekele, Berhan Solomon.   

Abstract

Weill Marchesani syndrome (WMS) is a rare condition characterized by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of the lens, severe myopia, and glaucoma. We report a typical case of WMS in an 18-year old female Ethiopian patient who presented with progressive visual loss from chronic angle closure glaucoma secondary to lens subluxation. Patients with WMS require early diagnosis in order to treat serious ocular and life-threatening systemic complications. To the best of our knowledge, only one case of the syndrome was previously reported in Africa.

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Year:  2009        PMID: 19743786

Source DB:  PubMed          Journal:  Ethiop Med J        ISSN: 0014-1755


  1 in total

Review 1.  Weill-Marchesani syndrome with advanced glaucoma and corneal endothelial dysfunction: a case report and literature review.

Authors:  Hui Guo; Xinyi Wu; Keli Cai; Zhi Qiao
Journal:  BMC Ophthalmol       Date:  2015-01-09       Impact factor: 2.209

  1 in total

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