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Primary hyperoxaluria detected by bone marrow biopsy: case report

BACKGROUND: Primary hyperoxaluria is a rare disease with an estimated prevalence of 1 to 3 cases per million. It is due to a hepatic enzyme deficiency responsible for an endogenous overproduction of oxalate. Oxalate crystals commonly deposit in the kidney and more rarely in bone marrow. The literatu...

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Detalles Bibliográficos
Autores principales: Nachite, F., Dref, M., Fakhri, A., Rais, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607598/
https://www.ncbi.nlm.nih.gov/pubmed/28943803
http://dx.doi.org/10.1186/s12907-017-0059-7