טוען...
Gastrointestinal Phenotype of Fabry Disease in a Patient with Pseudoobstruction Syndrome
Fabry disease is a rare, X-linked inborn error of glycosphingolipid metabolism caused by a deficiency of the lysosomal enzyme α-galactosidase A. Progressive deposition of GL-3 starts early in life, presumably as early as in fetal life. Chronic burning or provoked attacks of excruciating pain in hand...
שמור ב:
| Main Authors: | , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Springer Berlin Heidelberg
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3509874/ https://ncbi.nlm.nih.gov/pubmed/23430893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2011_63 |
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