Effect of acid-base changes on urinary hydrolases in Fabry's disease after renal transplantation

Fabry's disease, which is characterized by alpha-galactosidase A (AG) deficiency, causes early renal failure. Kidney transplants do not reliably supply the deficient enzyme. To assess both urinary excretion of AG by the transplant and the relationship between urine and serum hydrolase activity,...

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Bibliographic Details
Published in:	The Journal of laboratory and clinical medicine Vol. 115; no. 6; p. 696
Main Authors:	Berty, R M, Adler, S, Basu, A, Glew, R H
Format:	Journal Article
Language:	English
Published:	United States 01.06.1990
Subjects:	Adult alpha-N-Acetylgalactosaminidase Ammonium Chloride - therapeutic use beta-N-Acetyl-Galactosaminidase beta-N-Acetylhexosaminidases - urine Bicarbonates - therapeutic use Electrolytes - blood Electrolytes - urine Fabry Disease - enzymology Fabry Disease - surgery Fabry Disease - urine Glycoside Hydrolases - urine Hexosaminidases - urine Humans Hydrogen-Ion Concentration Kidney Transplantation Male Sodium - therapeutic use Sodium Bicarbonate Time Factors
ISSN:	0022-2143
Online Access:	Get more information
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