FABRY DISEASE: A CASE REPORT

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RAMEZANPOUR AFSHAR; FEIZI ABDOLAMIR; MOHAMMADI RAMIN

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Paper Information

Journal: Dermatology and Cosmetics Year:2011 | Volume:2 | Issue:1 Page(s): 64-67

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Information Journal Paper

Title

FABRY DISEASE: A CASE REPORT

Author(s)

RAMEZANPOUR AFSHAR | FEIZI ABDOLAMIR | MOHAMMADI RAMIN | Issue Writer Certificate

Keywords

FABRY DISEASEQ2

ANGIOKERATOMAQ3

NEPHROPATHYQ2

Abstract

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.

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APA: Copy

RAMEZANPOUR, AFSHAR, FEIZI, ABDOLAMIR, & MOHAMMADI, RAMIN. (2011). FABRY DISEASE: A CASE REPORT. DERMATOLOGY AND COSMETIC, 2(1), 64-67. SID. https://sid.ir/paper/157553/en

Vancouver: Copy

RAMEZANPOUR AFSHAR, FEIZI ABDOLAMIR, MOHAMMADI RAMIN. FABRY DISEASE: A CASE REPORT. DERMATOLOGY AND COSMETIC[Internet]. 2011;2(1):64-67. Available from: https://sid.ir/paper/157553/en

IEEE: Copy

AFSHAR RAMEZANPOUR, ABDOLAMIR FEIZI, and RAMIN MOHAMMADI, “FABRY DISEASE: A CASE REPORT,” DERMATOLOGY AND COSMETIC, vol. 2, no. 1, pp. 64–67, 2011, [Online]. Available: https://sid.ir/paper/157553/en

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