FAMILIALITY OF MONOCYTE ESTERASE DEFICIENCY IN PATIENTS ON CONTINUOUSAMBULATORY PERITONEAL-DIALYSIS

Citation
Dr. Hull et al., FAMILIALITY OF MONOCYTE ESTERASE DEFICIENCY IN PATIENTS ON CONTINUOUSAMBULATORY PERITONEAL-DIALYSIS, Renal failure, 20(4), 1998, pp. 607-612
Citations number
10
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
0886022X
Volume
20
Issue
4
Year of publication
1998
Pages
607 - 612
Database
ISI
SICI code
0886-022X(1998)20:4<607:FOMEDI>2.0.ZU;2-5
Abstract
The purpose of this study was to determine whether or not peripheral b lood monocyte esterase deficiency occurring in patients on CAPD was a familial characteristic The peripheral blood monocyte esterase status of 74 patients on CAPD was determined by a naphthyl acetate esterase s taining of cytospin preparations of their mononuclear cells following separation over ficoll. The peripheral blood of first degree relatives and spouses of monocyte esterase deficiency patients was similarly in vestigated for the deficiency. Three patients bad monocyte esterase de ficiency and familiality of the defect was demonstrated in two of thei r families. The third family was incompletely investigated because of lack of consent. The monocyte esterase deficiency demonstrated in this cohort of patients did not result from their renal failure but was a familial characteristic.