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先天性多发性关节挛缩症的神经性形式。3例完整尸检报告,包括首例报道的肌梭发育不全病例。

Neuropathic form of arthrogryposis multiplex congenita. Report of 3 cases with complete necropsy, including the first reported case of agenesis of muscle spindles.

作者信息

Krugliak L, Gadoth N, Behar A J

出版信息

J Neurol Sci. 1978 Jul;37(3):179-85. doi: 10.1016/0022-510x(78)90201-0.

Abstract

In 3 infants with arthrogryposis multiplex congenital (AMC) complete necropsy, including removal of the entire spinal cord, was performed. Histologically, spinal type (neurogenic) atrophy of skeletal muscles in conjunction with spinal motor neurone depletion, unaccompanied by noticeable gliosis, were the most preminent features common to all cases. In addition to these, one infant (Case 1) showed total absence of muscle spindles as evident from the examination of several hundred step-serial paraffin sections covering 11 different levels in 36 samples taken from a wide range of skeletal muscles of both upper and lower extremities. This is believed to be the first published case of agenesis of muscle spindles.

摘要

对3例患有先天性多发性关节挛缩症(AMC)的婴儿进行了完整的尸检,包括切除整个脊髓。组织学上,所有病例最突出的共同特征是骨骼肌的脊髓型(神经源性)萎缩并伴有脊髓运动神经元减少,且无明显的胶质细胞增生。除此之外,一名婴儿(病例1)经检查数百个连续石蜡切片后发现,取自上下肢广泛骨骼肌的36个样本在11个不同层面均完全没有肌梭。这被认为是首例发表的肌梭发育不全病例。

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