Liver-Kidney Transplantation in Primary Hyperoxaluria Type-1: Case Report and Literature Review
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a deficiency of the hepatic enzyme alanine-glyoxylate aminotransferase leads to endogenous oxalate overproduction, renal failure, systemic oxalate deposition and death. As hemodialysis provides insufficient...
| Main Authors: | , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Avicenna Organ Transplantation Institute
2011
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089259/ |