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American Journal of Roentgenology, Vol 100, 155-161, Copyright © 1967 by American Roentgen Ray Society

PRIMARY HYPEROXALURIA

ROENTGENOGRAPHIC, CLINICAL AND PATHOLOGIC FINDINGS

ALFRED L. WEBER M.D.1

1 Instructor in Radiology, Harvard Medical School; Assistant Radiologist, Massachusetts General Hosptal, Boston, Massachusetts

The case histories of 6 children with "primary hyperoxaluria" and the associated roentgenographic findings are presented.

This disorder is characterized by increased urinary excretion of oxalic and glycolic acids with formation of urinary tract stones and/or nephrocalcinosis.

The disease is most likely inherited as a recessive autosomal trait.

The symptoms are related to the urinary tract, and death, usually the result of uremia, often occurs in childhood or early adult life.

Roentgen studies demonstrate stones in the urinary tract or nephrocalcinosis with associated pyelonephritis.


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Copyright © 1967 by the American Roentgen Ray Society.