[MIM 613 616]

Very rare form of primary hyperoxaluria (< 5 %). Autosomal recessive transmission.

Mutation of the DHDPSL gene (10q24.2). Hyperoxaluria causing Ca oxalate lithiasis without oxalosis.

Anesthetic implications: 

urinary lithiasis; assure adequate perioperative hyperhydration.

References : 

Updated: March 2019