Giacoia G P, Hale J E
South Med J. 1984 Sep;77(9):1182-5. doi: 10.1097/00007611-198409000-00035.
We have described a family with X-linked myotubular myopathy that was clinically manifest in the neonatal period and compared it with the clinical picture and course of the disease in similar reported cases. Clinical expression of the disease in the newborn period is not always lethal. Despite a fatal outcome in the family reported here, a review of the literature indicates that aggressive treatment of short-term respiratory insufficiency at birth is justified.
我们描述了一个患有X连锁肌管性肌病的家族,该病在新生儿期出现临床症状,并将其与类似报道病例的临床表现和病程进行了比较。该疾病在新生儿期的临床表现并不总是致命的。尽管此处报道的家族出现了致命的结果,但文献回顾表明,对出生时的短期呼吸功能不全进行积极治疗是合理的。