Nocturnal Home Hemodialysis for a Patient With Type 1 Hyperoxaluria

Type 1 primary hyperoxaluria is a genetic disorder caused by deficiency of the liver-specific peroxisomal enzyme alanine-glyoxylate aminotransferase. This enzyme deficiency leads to excess oxalate production and deposition of calcium oxalate salts, resulting in kidney failure and systemic oxalosis....

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Veröffentlicht in:	American journal of kidney diseases 2013-12, Vol.62 (6), p.1155-1159
Hauptverfasser:	Plumb, Troy J., MD, Swee, Melissa L., MD, Fillaus, Jennifer A., DO
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Amino Acid Substitution - genetics Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Arginine - genetics Biological and medical sciences Circadian Rhythm Combined Modality Therapy dialysis DNA Mutational Analysis Emergency and intensive care: renal failure. Dialysis management Exons - genetics Female Glycine - genetics Hemodialysis, Home home hemodialysis Humans Hyperoxaluria, Primary - blood Hyperoxaluria, Primary - genetics Hyperoxaluria, Primary - therapy Intensive care medicine Kidney Failure, Chronic - blood Kidney Failure, Chronic - genetics Kidney Failure, Chronic - therapy Medical sciences Nephrology Nephrology. Urinary tract diseases oxalate Oxalates - blood Primary hyperoxaluria Pyridoxine - therapeutic use Transaminases - deficiency Transaminases - genetics
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