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AA Amyloidosis in a patient with glycogen storage disorder and progressive chronic kidney disease
Type 1 glycogen storage diseases (GSD) are inherited metabolic diseases caused by defects in the activity of the glucose-6-phosphate transporter. We present the case of a 40-year-old male with glycogen storage disease type 1b (GSD1b) who was referred to our nephrology service for evaluation of his c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400565/ https://www.ncbi.nlm.nih.gov/pubmed/26069801 http://dx.doi.org/10.1093/ckj/sfs143 |