Primary Hyperoxaluria Diagnosed Based on Bone Marrow Biopsy in Pancytopenic Adult with End Stage Renal Disease

Inborn errors of metabolism cause increase of metabolites in serum and their deposition in various organs including bone marrow. Primary hyperoxaluria (PH) is a rare inborn error in the pathway of glyoxylate metabolism which causes excessive oxalate production. The disease is characterized by widesp...

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Detalles Bibliográficos
Autores principales: Nematollahi, Pardis, Mohammadizadeh, Fereshteh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655042/
https://www.ncbi.nlm.nih.gov/pubmed/26634160
http://dx.doi.org/10.1155/2015/402947

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655042/
https://www.ncbi.nlm.nih.gov/pubmed/26634160
http://dx.doi.org/10.1155/2015/402947

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