Fabry disease previously diagnosed as Henoch-Schonlein purpura.
10.3904/kjim.2015.30.6.925
- Author:
Ji Hyeong KIM
1
;
Dong Hoon HAN
;
Moo Yong PARK
;
Soo Jeong CHOI
;
Jin Kuk KIM
;
Seung Duk HWANG
;
So Young JIN
Author Information
1. Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea. crystal@schmc.ac.kr
- Publication Type:Case Reports ; Letter ; Research Support, Non-U.S. Gov't
- Keywords:
Alpha-galactosidase;
Fabry disease;
Purpura, Schoenlein-Henoch
- MeSH:
Biopsy;
DNA Mutational Analysis;
*Diagnostic Errors;
Enzyme Replacement Therapy;
Fabry Disease/complications/*diagnosis/enzymology/genetics;
Genetic Predisposition to Disease;
Glomerulonephritis, IGA/diagnosis/etiology;
Humans;
Male;
Middle Aged;
Mutation;
Phenotype;
Predictive Value of Tests;
Purpura, Schoenlein-Henoch/*diagnosis;
alpha-Galactosidase/genetics/therapeutic use
- From:The Korean Journal of Internal Medicine
2015;30(6):925-927
- CountryRepublic of Korea
- Language:English
-
Abstract:
No abstract available.
