de Goede Christian G E L, Kelsey Anna, Kingston Helen, Tomlin Pamela I, Hughes M Imelda
Paediatric Neurology, Royal Preston Hospital, Preston, UK.
Dev Med Child Neurol. 2005 Dec;47(12):835-7. doi: 10.1017/S0012162205001763.
In children with a myopathy, muscle biopsy, together with the clinical presentation, can guide further investigations. The presence of centrally located nuclei suggests a myotubular myopathy, and gene testing may confirm this diagnosis. We describe a male child with a mild form of X-linked myotubular myopathy for which repeated muscle biopsy did not show the characteristic pattern of centrally located nuclei. Myotubular myopathy was not contemplated, therefore, until a maternally related relative was shown to have the disorder. Genetic testing showed that the index case carried the same mutation in his MTM1 gene as this relative.
对于患有肌病的儿童,肌肉活检结合临床表现可指导进一步检查。中央核的存在提示为肌管型肌病,基因检测可证实这一诊断。我们描述了一名患有轻度X连锁肌管型肌病的男童,其重复进行的肌肉活检未显示中央核的特征性模式。因此,在发现一名母系亲属患有该疾病之前,并未考虑到肌管型肌病。基因检测显示,该索引病例在其MTM1基因中携带与这名亲属相同的突变。