Lundemo G, Laerdal A
Klinisk neurofysiologisk laboratorium, Sentralsjukehuset i Rogaland, Stavanger.
Tidsskr Nor Laegeforen. 1992 Jun 10;112(15):1954-5.
Congenital myotonic dystrophy is a distinct entity causing severe hypotonia and other neuromuscular manifestations. The disease is usually inherited from the mother and shows a more severe course than the adult form of dystrophia myotonica. Congenital myotonic dystrophy is associated with increased perinatal mortality. We describe a case with this disorder and discuss the differential diagnosis in relation to other neuromuscular disorders causing hypotonia in early life.
先天性肌强直性营养不良是一种导致严重肌张力减退及其他神经肌肉表现的独特病症。该疾病通常由母亲遗传,且病程比成人型肌强直性营养不良更为严重。先天性肌强直性营养不良与围产期死亡率增加相关。我们描述了一例患有这种疾病的病例,并讨论了与其他在生命早期导致肌张力减退的神经肌肉疾病相关的鉴别诊断。