Cargando…
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: | Dick, Jonathan, Kumar, Nicola, Horsfield, Catherine, Jayawardene, Satish |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
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 |
Ejemplares similares
-
AA amyloidosis in the renal allograft: a report of two cases and review of the literature
por: Rojas, Rebecca, et al.
Publicado: (2012) -
Post COVID-19 AA amyloidosis of the kidneys with rapidly progressive renal failure
por: Mir, Tajamul H., et al.
Publicado: (2023) -
Desmopressin use prior to renal transplant biopsy—does it fit?
por: Anandagoda, Nelomi, et al.
Publicado: (2014) -
Kidney dysfunction due to AA amyloidosis in a morbidly obese female
por: Izzedine, Hassan, et al.
Publicado: (2023) -
AA amyloidosis and pyrin gene mutations
por: Konstantopoulos, K., et al.
Publicado: (2005)