McMenamin J B, Curry B, Taylor G P, Becker L E, Murphy E G
Can J Neurol Sci. 1984 May;11(2):305-9. doi: 10.1017/s0317167100045583.
The clinical and neuropathological findings in two infants with congenital nemaline myopathy are described. One patient presented at birth with severe hypotonia, respiratory failure and contractures and died shortly after the neonatal period. The other presented at age two months with hypotonia and, following a period of clinical stability, died at age seven months from respiratory failure. Pathological findings in the fatal neonatal case revealed numerous rod bodies in lingual, pharyngeal, diaphragm and limb muscles, correlating with clinical findings. Significant, but less rod body involvement was found in the diaphragm and limb muscles of the second patient. Although a neural basis has been suggested for this disorder, no abnormalities were found in the central nervous system or in the peripheral nerves of these two severely affected patients.
本文描述了两名先天性杆状体肌病婴儿的临床和神经病理学发现。一名患者出生时即出现严重肌张力减退、呼吸衰竭和挛缩,新生儿期后不久死亡。另一名患者在两个月大时出现肌张力减退,在经历一段临床稳定期后,于七个月大时死于呼吸衰竭。致命新生儿病例的病理发现显示,舌肌、咽肌、膈肌和肢体肌肉中有大量杆状体,与临床表现相关。在第二名患者的膈肌和肢体肌肉中发现了明显但较少的杆状体受累情况。尽管有人提出这种疾病存在神经学基础,但在这两名严重受影响患者的中枢神经系统或周围神经中未发现异常。