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Anaesthesiologic protocol for kidney transplantation in two patients with Fabry Disease: a case series
Fabry's Disease is a rare genetic syndrome, with a classic X-linked alpha -galactosidase A deficiency phenotype, responsible for glico-sphyngolypids metabolism impairment with clinical effects in several organs and functions. We describe the anaesthesiologic implications of two patients with Fa...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2008
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2596113/ https://ncbi.nlm.nih.gov/pubmed/19014714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-1-321 |
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