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A Cardiac Variant of Fabry Disease Diagnosed with Chance Urinary Mulberry Cells
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of α-galactosidase A and is classified into two types: classical and variant. The classical type exhibits classic manifestations, but the variant type does not and is therefore difficult to identify sometimes. A 73-year-o...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Japanese Society of Internal Medicine
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306526/ https://www.ncbi.nlm.nih.gov/pubmed/29984754 http://dx.doi.org/10.2169/internalmedicine.1177-18 |