%0 Journal Article
%T Primary Hyperoxaluria Type 1 with Thrombophilia in Pregnancy: A Case Report
%A Asma Hasan
%A Dominick Santoriello
%A Henry Schairer
%A Sharon Maynard
%J Archive of "Case Reports in Nephrology and Dialysis".
%D 2018
%R 10.1159/000493091
%X Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease caused by a mutation in the AGXT gene, resulting in deficiency of the alanineglyoxylate:aminotransferase enzyme. It is characterized by accumulation of oxalate in the kidneys and other organs
%K Primary hyperoxaluria
%K Pregnancy
%K Thrombophilia
%K Nephrolithotomy
%K Nephrolithiasis
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206957/