Paraplegia as a presentation of primary hyperoxaluria

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Primary Hyperoxaluria

Primary hyperoxalurias are rare recessive inherited inborn errors of glyoxylate metabolism. They are responsible for progressive renal involvement, which further lead to systemic oxalate deposition, which can even occur in infants. Primary hyperoxaluria type 1 is the most common form in Europe and is due to alanine-glyoxylate aminostransferase deficiency, a hepatic peroxisomal pyridoxin-depende...

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ژورنال

عنوان ژورنال: CEN Case Reports

سال: 2018

ISSN: 2192-4449

DOI: 10.1007/s13730-018-0349-7