Goto I, Muraoka S, Fujii N, Ohta M, Kuroiwa Y
J Neurol. 1981;226(2):143-8. doi: 10.1007/BF00313443.
A case is described with the characteristic clinical features of rigid spine syndrome: childhood onset in a male, very slowly progressive weakness and muscle atrophy, limitation of neck and trunk flexion, joint contractures, normal intelligence, no clear family history, increased serum CPK levels and myopathic patterns in EMG and muscle biopsy specimens. Myopathic patterns with various histological changes in muscle biopsy specimens were seen in all eight reported cases of the rigid spine syndrome, but there are no characteristic histological findings in the rigid spine syndrome.
男性儿童期起病,肌无力和肌肉萎缩进展极为缓慢,颈部和躯干前屈受限,关节挛缩,智力正常,无明确家族史,血清肌酸磷酸激酶(CPK)水平升高,肌电图和肌肉活检标本显示肌病模式。在已报道的所有8例僵硬脊柱综合征病例中,肌肉活检标本均可见具有各种组织学改变的肌病模式,但僵硬脊柱综合征并无特征性的组织学表现。