Ocular manifestations of Gaucher disease: case report and literature review
We report the case of a patient with Gaucher disease (GD) type 3b, with a homozygous GBA gene mutation (c.1448T > C p.L483P) (L444P). Ocular findings characteristic of this mutation are described, including vitreous condensation and macular edema. To our knowledge this is the first case reported...
Main Authors: | , , , , |
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Format: | Article |
Language: | Spanish |
Published: |
Universidad de Antioquia
2017-07-01
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Series: | Iatreia |
Subjects: | |
Online Access: | http://aprendeenlinea.udea.edu.co/revistas/index.php/iatreia/article/view/26728/20785179 |