Cummings J F, Cooper B J, de Lahunta A, van Winkle T J
Acta Neuropathol. 1981;53(2):137-43. doi: 10.1007/BF00689994.
A recessively inherited hypertrophic neuropathy was discovered in Tibetan Mastiff dogs. Affected pups developed a generalized weakness with hyporeflexia shortly after weaning. Diagnostic findings in 10-18-week-old pups included: moderate to severe reduction in nerve conduction velocities, infrequent denervation potentials, and inconstant elevation in CSF protein. Light- and electron-microscopic studies of peripheral nerves and roots revealed widespread demyelination and primitive onion bulb formation with relatively little degeneration of axons. Myelin changes often were most striking in the cytoplasmic regions of the sheaths and consisted of separations at the major dense lines, anomalous incisure patterns, and marked filamentous accumulations in the inner spirals and adaxonal cytoplasm. The results of these initial studies suggest an inborn defect in the Schwann cell's ability to form or maintain a stable myelin sheath.
在藏獒中发现了一种隐性遗传的肥厚性神经病变。患病幼犬在断奶后不久就会出现全身无力和反射减退。10至18周龄幼犬的诊断结果包括:神经传导速度中度至重度降低、偶见失神经电位以及脑脊液蛋白含量不定升高。对周围神经和神经根的光镜和电镜研究显示广泛的脱髓鞘和原始洋葱球形成,轴突退变相对较少。髓鞘变化在鞘的细胞质区域通常最为明显,表现为主要致密线处的分离、异常的切迹模式以及内螺旋和轴突旁细胞质中明显的丝状积聚。这些初步研究结果表明雪旺氏细胞形成或维持稳定髓鞘的能力存在先天性缺陷。