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- C Sommer, N Uçeyler, T Duning, K Arning, R Baron, E Brand, S Canaan-Kühl, M Hilz, D Naleschinski, C Wanner, and F Weidemann.
- Neurologische Klinik, Universitätsklinikum Würzburg, Deutschland. sommer@uni-wuerzburg.de
- Internist (Berl). 2013 Jan 1; 54 (1): 121-2, 124-30.
AbstractFabry's disease is an X-chromosome linked lysosomal storage disorder with α-galactosidase A deficiency and subsequent multiple organ involvement. An early and common symptom also in later stages of the disease is pain. This pain depends on various precipitating factors and can severely compromise the quality of life. So-called Fabry crises can lead to the necessity for intensive care treatment. The pain can be classified as predominantly neuropathic and is difficult to treat. In addition, medication has to be adjusted to concomitant cardiac and renal involvement in Fabry's disease. This review gives guidance for pain therapy in Fabry's disease based on the available evidence and on experience.
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