Telerman-Toppet N, Khoubesserian P, Bacq M, Durdu J, Lambelin D, Lousberg G, Coërs C
Muscle Nerve. 1984 Jul-Aug;7(6):439-41. doi: 10.1002/mus.880070604.
A familial myopathy with predominantly proximal muscle atrophy is described. Although several clinical features such as sternomastoid and brachioradialis muscle involvement suggested Steinert disease, myotonia was not demonstrated by clinical examination or EMG. Histological data were consistent with myotonic dystrophy.
本文描述了一种以近端肌肉萎缩为主的家族性肌病。尽管胸锁乳突肌和肱桡肌受累等一些临床特征提示为斯坦纳特病，但临床检查或肌电图均未发现肌强直。组织学数据与强直性肌营养不良一致。
