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...

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Detalles Bibliográficos
Autores principales: Siegal, D., Su, W. S., DaBreo, D., Puglia, M., Gregor, L., Gangji, A. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Organ Transplantation Institute 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089259/
https://www.ncbi.nlm.nih.gov/pubmed/25013605

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089259/
https://www.ncbi.nlm.nih.gov/pubmed/25013605

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