RECURRENT CONGENITAL ARTHROGRYPOSIS LEADING TO A DIAGNOSIS OF MYASTHENIA-GRAVIS IN AN INITIALLY ASYMPTOMATIC MOTHER

被引:28
作者
BARNES, PRJ
KANABAR, DJ
BRUETON, L
NEWSOMDAVIS, J
HUSON, SM
MANN, NP
HILTONJONES, D
机构
[1] UNIV OXFORD,RADCLIFFE INFIRM,DEPT CLIN NEUROL,OXFORD OX2 6HE,ENGLAND
[2] ROYAL BERKSHIRE HOSP,BUSCOT NEONATAL INTENS CARE UNIT,READING RG1 5AN,BERKS,ENGLAND
[3] CHURCHILL HOSP,DEPT MED GENET,OXFORD OX3 7LJ,ENGLAND
[4] NORTHWICK PK HOSP & CLIN RES CTR,DEPT MED GENET,HARROW,MIDDX,ENGLAND
关键词
MYASTHENIA GRAVIS; NEONATAL; CONGENITAL ARTHROGRYPOSIS; NEUROMUSCULAR JUNCTION; PLASMAPHERESIS; GENETIC COUNSELING;
D O I
10.1016/0960-8966(94)E0029-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report a sibship in which the syndrome of congenital arthrogryposis occurred in two male and two female neonates, three of whom died. The mother was asymptomatic at the time of the first pregnancy and the subsequent development of muscle weakness was later confirmed to be due to myasthenia gravis. The literature on this association is briefly reviewed and the extremely high risk of recurrence of this complication in subsequent pregnancies is addressed.
引用
收藏
页码:59 / 65
页数:7
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