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Primary Hyperoxaluria in Infancy.

Authors :
SRINIVAS, H.N.
RAMKUMAR, CHANDRAN
Source :
Australasian Radiology; 1986, Vol. 30 Issue 4, p332-334, 3p
Publication Year :
1986

Abstract

ABSTRACT Primary Hyperoxaluria is a rare autosomal recessive disorder causing progressive renal failure and death before adulthood in most cases<superscript>1</superscript>. Acute renal failure due to Primary Hyperoxaluria with renal oxalosis is rare in infancy<superscript>2</superscript>- <superscript>3</superscript> and we report such a case emphasizing the importance of ultrasonographic examination in the diagnosis of this condition. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00048461
Volume :
30
Issue :
4
Database :
Complementary Index
Journal :
Australasian Radiology
Publication Type :
Academic Journal
Accession number :
90967909
Full Text :
https://doi.org/10.1111/j.1440-1673.1986.tb01766.x