Volume 2, Issue 1 (3-2011)
jdc 2011, 2(1): 64-67 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Ramezanpour A, Feizi A, Mohammadi R. Fabry disease. jdc 2011; 2 (1) :64-67
URL: http://jdc.tums.ac.ir/article-1-41-en.html
URL: http://jdc.tums.ac.ir/article-1-41-en.html
Abstract: (23622 Views)
Fabry disease is a X-linked lysosomal storage disorder due to alpha galactosidase A deficiency leading to abnormal accumulation of glycosphingolipids in different parts of body. This case report introduces a 35-year-old man with diffuse keratotic erythematous papules. Histopathological evaluation of the skin biopsy suggested the diagnosis of angiokeratoma. With attention to his nephropathy and the same skin lesions and renal involvement in his brother, which led him to receive renal transplantation, the diagnosis of Fabry disease was suggested.
Type of Study: Research |
Subject:
General
Received: 2011/01/3 | Accepted: 2011/02/16 | Published: 2013/07/16
Received: 2011/01/3 | Accepted: 2011/02/16 | Published: 2013/07/16
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
