Sabouraud O, Pinel J F, Le Bars R, Menault F, Saudeau D
Rev Neurol (Paris). 1979 Oct;135(8-9):583-92.
The symptom described as muscle weakness corrected by exercise appears to be part of the recessive form of congenital myotonia, of which it can constitute the dominant clinical manifestation in some cases. This symptom coincides with decrements of the action of potentials to repetitive stimulations in the electromyogram, which may be particularly severe in these same cases. These observations contribute to the modification and precision of the description of the recessive form of Thomsen's disease, but their pathogenicity remains unclear.
被描述为运动可纠正的肌无力症状似乎是先天性肌强直隐性形式的一部分,在某些情况下,它可能构成主要临床表现。该症状与肌电图中对重复刺激的动作电位衰减相吻合,在这些相同病例中可能尤为严重。这些观察结果有助于对汤姆森病隐性形式的描述进行修正和精确化,但其致病性仍不明确。