Descrizione
Pathophysiology of Anderson-Fabry disease and its gastrointestinal manifestations are illustrated, showing how alpha-galactosidase A deficiency leads to glycosphingolipid accumulation in GI tissues.
Figure 1
DiagramSource Paper
Gastrointestinal Involvement in Anderson-Fabry Disease: A Narrative Review.International journal of environmental research and public health (2021)
PMID: 33807115
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![Figure 1: Pathophysiology of Anderson-Fabry disease and its gastrointestinal manifestations are illustrated, showing how alpha-galactosidase A deficiency leads to glycosphingolipid accumulation in GI tissues.]() > Source: Fabio Caputo et al. "Gastrointestinal Involvement in Anderson-Fabry Disease: A Narrative Review.." *International journal of environmental research and public health*, 2021. PMID: [33807115](https://pubmed.ncbi.nlm.nih.gov/33807115/)
<figure> <img src="" alt="Pathophysiology of Anderson-Fabry disease and its gastrointestinal manifestations are illustrated, showing how alpha-galactosidase A deficiency leads to glycosphingolipid accumulation in GI tissues." /> <figcaption>Figure 1. Pathophysiology of Anderson-Fabry disease and its gastrointestinal manifestations are illustrated, showing how alpha-galactosidase A deficiency leads to glycosphingolipid accumulation in GI tissues.<br> Source: Fabio Caputo et al. "Gastrointestinal Involvement in Anderson-Fabry Disease: A Narrative Review.." <em>International journal of environmental research and public health</em>, 2021. PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/33807115/">33807115</a></figcaption> </figure>