BOVINE BETA-MANNOSIDASE DEFICIENCY

被引:24
作者
BRYAN, L
SCHMUTZ, S
HODGES, SD
SNYDER, FF
机构
[1] UNIV CALGARY,DEPT PEDIAT & MED BIOCHEM,CALGARY T2N 4N1,ALBERTA,CANADA
[2] ALBERTA DEPT AGR,REG VET LAB,AIRDRIE T4B 2C1,ALBERTA,CANADA
[3] UNIV SASKATCHEWAN,DEPT ANIM & POULTRY SCI,SASKATOON S7N 0W0,SASKATCHEWAN,CANADA
关键词
D O I
10.1016/S0006-291X(05)80060-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A fatal inherited glycoprotein storage disorder is described in Salers cattle which affects both sexes. Affected calves are unable to stand at birth, have a marked intention tremor, markedly enlarged kidneys, decreased white matter in all areas of the brain, and cytoplasmic vacuolation in multiple cell types of multiple tissues with nervous, renal, lymphoid and thyroid tissues most severely affected. Affected calves were grossly deficient in lymphocyte and brain β-mannosidase activity and had markedly reduced but not deficient activity in liver and kidney. A test mating of obligate carriers produced three genotypes: affected, carrier, non-carrier in essentially the expected ratio of 1:2:1, consistent with autosomal recessive inheritance. © 1990 Academic Press, Inc.
引用
收藏
页码:491 / 495
页数:5
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